Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan von Iqbal, Afia, Naz, Shagufta, Kaul, Haiba, Sharif, Saima, Khushbakht, Aysha, Naeem, Muhammad Asif, Iqtedar, Mehwish, Kaleem, Afshan, Firasat, Sabika, Manzoor, Farkhanda

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Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan von Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor

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SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families von Firasat, Sabika, Dur-e-Shawar, Khan, Wajid Ali, Sughra, Ume, Nousheen, Kaul, Haiba, Naz, Shagufta, Noreen, Bushra, Gul, Rutaba, Afshan, Kiran

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Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family von Jiao, Xiaodong, Khan, Shahid Y, Kaul, Haiba, Butt, Tariq, Naeem, Muhammad Asif, Riazuddin, Sheikh, Hejtmancik, J Fielding, Riazuddin, S Amer

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Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site... von Afzal, Rabia, Firasat, Sabika, Kaul, Haiba, Ahmed, Bashir, Siddiqui, Sorath N., Zafar, Saemah N., Shahzadi, Misbah, Afshan, Kiran

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Clinical profile and screening of exon 6 and 14 of ABCB4 gene in obstetric cholestasis patients at a tertiary care hospital in Rawalpindi, Pakistan von Noor, Nuzhat, Firasat, Sabika, Bano, Naheed, Afshan, Kiran, Gul, Bushra, Kaul, Haiba

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Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts von Irum, Bushra, Khan, Shahid Y, Ali, Muhammad, Kaul, Haiba, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Nadeem, Raheela, Khan, Arif O, Al Obaisi, Saif, Naeem, Muhammad Asif, Nasir, Idrees A, Khan, Shaheen N, Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O, Riazuddin, S Amer

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Homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene von Shakil, Muhammad, Ullah, Muhammad Ikram, Hussain, Shabbir, Firasat, Sabika, Mahmood, Saqib, Kaul, Haiba

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Genetic insights into crossbred dairy cattle of Pakistan: exploring allele frequency, linkage disequilibrium, and effective population size at a genome-wide scale von Nisa, Fakhar un, Kaul, Haiba, Asif, Muhammad, Amin, Imran, Mrode, Raphael, Mansoor, Shahid, Mukhtar, Zahid

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Genetic Polymorphism and serum levels of Insulin like Growth Factor-1 (Igf-1) in patients of rheumatoid arthritis von Fayyaz, Iram, Khaliq, Saba, Bano, Farhat, Kaul, Haiba

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Correction: Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan von Iqbal, Afia, Naz, Shagufta, Kaul, Haiba, Sharif, Saima, Khushbakht, Aysha, Naeem, Muhammad Asif, Iqtedar, Mehwish, Kaleem, Afshan, Firasat, Sabika, Manzoor, Farkhanda

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Determination of Serum Trace Elements (Zn, Cu, and Fe) in Pakistani Patients with Rheumatoid Arthritis von Ullah, Zia, Ullah, Muhammad Ikram, Hussain, Shabbir, Kaul, Haiba, Lone, Khalid P.

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Fine mapping of chromosome 9 locus associated with congenital cataract von Kaul, Haiba, Hussain, Shabbir, Mustafa, Ghulam, Naz, Shagufta

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Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene von Shahzadi, Misbah, Firasat, Sabika, Kaul, Haiba, Afshan, Kiran, Afzal, Rabia, Naz, Shagufta

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Prevalence of stromal corneal dystrophies in Lahore von Naz, Shagufta, Sharif, Saima, Kaul, Haiba, Kaleem, Afshan, Tehseen, Amina

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In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma von Firasat, Sabika, Kaul, Haiba, Ashfaq, Usman Ali, Idrees, Sobia

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Delineating Novel and Known Pathogenic Variants in TYR , OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families von Shakil, Muhammad, Akbar, Abida, Aisha, Nazish Mahmood, Hussain, Intzar, Ullah, Muhammad Ikram, Atif, Muhammad, Kaul, Haiba, Amar, Ali, Latif, Muhammad Zahid, Qureshi, Muhammad Atif, Mahmood, Saqib

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Missense mutation in SLC4A11 in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2) von Kaul, Haiba, Suman, Maryam, Khan, Zoya, Ullah, Muhammad Ikram, Ashfaq, Usman Ali, Idrees, Sobia

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Correction: Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan von Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor

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Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family von Kaul, Haiba, Riazuddin, S Amer, Shahid, Mariam, Kousar, Samra, Butt, Nadeem H, Zafar, Ahmad U, Khan, Shaheen N, Husnain, Tayyab, Akram, Javed, Hejtmancik, J Fielding, Riazuddin, Sheikh

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