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Molecular basis of splotch and Waardenburg Pax-3 mutations.

Pax genes control certain aspects of development, as mutations result in (semi)dominant defects apparent during embryogenesis. Pax-3 has been associated with the mouse mutant splotch (Sp) and the human Waardenburg syndrome type 1 (WS1). We have examined the molecular basis of splotch and WS1 by stud...

詳細記述

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書誌詳細
主要な著者: Chalepakis, G, Goulding, M, Read, A, Strachan, T, Gruss, P
フォーマット: Artigo
言語:Inglês
出版事項: 1994
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC43646/
https://ncbi.nlm.nih.gov/pubmed/7909605
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