A rare case of congenital fibrosis of extraocular muscle...

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European Journal of Paediatric Neurology 2015 / 7

A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon

Kaçar Bayram, Ayşe, Per, Hüseyin, Quon, Jennifer, Canpolat, Mehmet, Ülgen, Ege, Doğan, Hakkı, Gumus, Hakan, Kumandas, Sefer, Bayram, Nurettin, Bilguvar, Kaya, Çağlayan, Ahmet Okay
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Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2015.06.003
Date:
July, 2015
File:
PDF, 479 KB
english, 2015
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