Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis von Sleiman, Maria Bou, Sleiman, Maroun Bou, Abbas, Ossama, Btadini, Waed, Najjar, Tracy, Tofaili, Mona, Chedraoui, Adele, Khalil, Samar, Kibbi, Abdul Ghani, Kurban, Mazen

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A Homozygous Frameshift Mutation in the HOXC13 Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family von Farooq, Muhammad, Kurban, Mazen, Fujimoto, Atsushi, Fujikawa, Hiroki, Abbas, Ossama, Nemer, Georges, Saliba, Jessica, Sleiman, Rima, Tofaili, Mona, Kibbi, Abdul-Ghani, Ito, Masaaki, Shimomura, Yutaka

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Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis von Sleiman, Maria Bou, Sleiman, Maroun Bou, Abbas, Ossama, Btadini, Waed, Najjar, Tracy, Tofaili, Mona, Chedraoui, Adele, Khalil, Samar, Kibbi, Abdul Ghani, Kurban, Mazen

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