Mutations of PAX3 unlikely in Waardenburg syndrome type 2.
作者信息
Arias S
出版信息
Nat Genet. 1993 Sep;5(1):8. doi: 10.1038/ng0993-8a.
PMID:8220430
Abstract
摘要
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[Unilateral sensineural deafness associated with mutations in the PAX3-gene in Waardenburg syndrome type I].
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