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

✍ Scribed by Hilde Van Esch; Anna Jansen; Marijke Bauters; Guy Froyen; Jean-Pierre Fryns

Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 121 KB
Volume: 143A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31572

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