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A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome

✍ Scribed by U. Koppelhus; L. Tranebjærg; G. Esberg; M. Ramsing; M. Lodahl; N. D. Rendtorff; H. V. Olesen; M. Sommerlund

Book ID: 108696812
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 487 KB
Volume: 36
Category: Article
ISSN: 0307-6938
DOI: 10.1111/j.1365-2230.2010.03936.x

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