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De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome

✍ Scribed by Araceli Álvarez; Ignacio del Castillo; Alejandra Pera; Manuela Villamar; Miguel A. Moreno-Pelayo; Felipe Moreno; Ramón Moreno; M. Cruz Tapia

Publisher: John Wiley and Sons
Year: 2002
Tongue: English
Weight: 100 KB
Volume: 117A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.10851

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