tailieunhanh - Identification of a mutation in a Vietnamese family with Emery-Dreifuss muscular dystrophy using whole exome sequencing

The clinical presentations of each patient in this study are different from each other, demonstrating the intrafamilial phenotypic variability of this mutation. Early identification of the underlying genetic course of the disease by sequencing, combined with clinical findings provides solid evidence to diagnosis process, genetic counseling and management strategy. |

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