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Supplement: 41392_2024_1960_MOESM6_ESM.xlsx › Table_S5
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Supplement: 41417_2021_347_MOESM4_ESM.xls › C000-ZZP8UU
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
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Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
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