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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.

Ghulam Mujtaba,Julie M Schultz,Ayesha Imtiaz,Robert J Morell,Thomas B Friedman,Sadaf Naz

JOURNAL OF MEDICAL GENETICS（2015）

引用 34|浏览12
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关键词
genetics,genome-wide,linkage,molecular genetics
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