Whole Exome Sequencing Identified a 13 Base Pair MYH7 Deletion-mutation in a Patient With Restrictive Cardiomyopathy and Left Ventricle Hypertrophy
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Whole Exome Sequencing Identified a 13 Base Pair MYH7 Deletion-mutation in a Patient With Restrictive Cardiomyopathy and Left Ventricle Hypertrophy
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