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Delineation of the clinical phenotype associated with OPHN1 mutations based on the clinical and neuropsychological evaluation of three families

✍ Scribed by B. Chabrol; N. Girard; K. N'Guyen; A. Gérard; M. Carlier; L. Villard; Nicole Philip

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 177 KB
Volume: 138A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.30882

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