Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent von Chakravorty, Samya, Nallamilli, Babi Ramesh Reddy, Khadilkar, Satish Vasant, Singla, Madhu Bala, Bhutada, Ashish, Dastur, Rashna, Gaitonde, Pradnya Satish, Rufibach, Laura E, Gloster, Logan, Hegde, Madhuri

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Genetic Appraisal of Hereditary Muscle Disorders In A Cohort From Mumbai, India von Khadilkar, Satish Vasant, Halani, Hiral Amrut, Dastur, Rashna, Gaitonde, Pradnya Satish, Oza, Harsh, Hegde, Madhuri

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Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm:... von Dastur, Rashna Sam, Gaitonde, Pradnya Satish, Kachwala, Munira, Nallamilli, Babi R R, Ankala, Arunkanth, Khadilkar, Satish V, Atchayaram, Nalini, Gayathri, N, Meena, A K, Rufibach, Laura, Shira, Sarah, Hegde, Madhuri

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Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients von Dastur Rashna S, Gaitonde Pradnya S, Khadilkar Satish V, Udani Vrajesh P, Nadkarni Jayshree J

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Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients von Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Tanner, Alice, Ankala, Arunkanth, Schneider, Thomas, da Silva, Cristina, Beadling, Randall, Alexander, John J., Askree, Syed Hussain, Whitt, Zachary, Bean, Lora, Collins, Christin, Khadilkar, Satish, Gaitonde, Pradnya, Dastur, Rashna, Wicklund, Matthew, Mozaffar, Tahseen, Harms, Matthew, Rufibach, Laura, Mittal, Plavi, Hegde, Madhuri

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Early and consistent pattern of proximal weakness in GNE myopathy von Khadilkar, Satish V., Chaudhari, Amit D., Singla, Madhu B., Dastur, Rashna S., Gaitonde, Pradnya S., Bhutada, Ashish G., Hegde, Madhuri R.

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Limb-girdle muscular dystrophy in the Agarwals: Utility of founder mutations in CAPN3 gene von Khadilkar, Satish V, Chaudhari, Chetan R, Dastur, Rashna S, Gaitonde, Pradnya S, Yadav, Jayendra G

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Ancestral founder mutations in calpain-3 in the Indian Agarwal community: Historical, clinical, and molecular perspective von Ankala, Arunkanth, Kohn, Jordan N., Dastur, Rashna, Gaitonde, Pradnya, Khadilkar, Satish V., Hegde, Madhuri R.

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Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain... von Dastur, Rashna S, Kachwala, Munira Y, Khadilkar, Satish V, Hegde, Madhuri R, Gaitonde, Pradnya S

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Becker muscular dystrophy in Indian patients: Analysis of dystrophin gene deletion patterns von Dastur, Rashna S, Gaitonde, Pradnya S, Khadilkar, Satish V, Nadkarni, Jayshree J

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Duchenne and Becker muscular dystrophies: An Indian update on genetics and rehabilitation von Nadkarni, Jayshree J, Dastur, Rashna S, Viswanathan, V, Gaitonde, Pradnya S, Khadilkar, Satish V

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Clinical and genomic evaluation of 207 genetic myopathies in the Indian subcontinent von Chakravorty, Samya, Nallamilli, Babi, Khadilkar, Satish, Singla, Madhu Bala, Bhutada, Ashish, Dastur, Rashna, Gaitonde, Pradnya, Rufibach, Laura, Gloster, Logan, Hegde, Madhuri

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