Encephalopathy and bilateral cataract in a boy with an...

American Journal of Medical Genetics Part A 2007 Vol. 143A; Iss. 4

Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes

Hilde Van Esch, Anna Jansen, Marijke Bauters, Guy Froyen, Jean-Pierre Fryns
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Volume:
143A
Year:
2007
Language:
english
Pages:
6
DOI:
10.1002/ajmg.a.31572
File:
PDF, 121 KB
english, 2007
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