Massoumeh Ramahi
Mashhad,
Abstracts, Massoumeh Ramahi [Author]
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21A gene c.2860C>T mutation in CFEOM1A: first case report from Iran
Medical GeneticsCongenital fibrosis of the extraocular muscles1A (CFEOM1A) is an autosomal dominant condition characterized by ophthalmo...Read more