4 results on '"Shahzad, Mohsin"'
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2. Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss
3. Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
4. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p
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