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A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E

✍ Scribed by Laurence Jonard; Delphine Feldmann; Christophe Parsy; Sylvie Freitag; Martine Sinico; Céleste Koval; Mhamed Grati; Remy Couderc; Françoise Denoyelle; Christine Bodemer; Sandrine Marlin; Smail Hadj-Rabia

Book ID: 116433060
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 493 KB
Volume: 51
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2007.09.005

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