Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.1

X-linked albinism-deafness syndrome (ADFN) was described in one Israeli Jewish family and is characterized by congenital nerve deafness and piebaldness. The ADFN mutation probably affects the migration of neural crest–derived precursors of the melanocytes. As a first step toward identifying the ADFN...

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Main Authors: Shiloh, Yosef, Litvak, Gilad, Ziv, Yael, Lehner, Thomas, Sandkuyl, Lodewijk, Hildesheimer, Minka, Buchris, Vered, Cremers, Frans P. M., Szabo, Paul, White, Bradley N., Holden, Jeanette J. A., Ott, Jurg
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683749/
https://ncbi.nlm.nih.gov/pubmed/2349949
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