Putative Digenic < b > < i > GJB2/MYO7A < /i > < /b > Inheritance of Hearing Loss Detected in a Patient with 48,XXYY Klinefelter Syndrome

Conclusions: Our findings reported a putativeGJB2/MYO7A digenic inheritance form of hearing loss, expanding the genotype and phenotype spectrum of NSHL. In addition, this is the first report of concomitant NSHL and 48,XXYY syndrome.Hum Hered
Source: Human Heredity - Category: Genetics & Stem Cells Source Type: research