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pro vyhledávání: '"Duaa M. Al-Majmaie"'
Autor:
Michelle V. Tomczewski, John Z. Chan, Duaa M. Al-Majmaie, Ming Rong Liu, Alex D. Cocco, Ken D. Stark, Douglas Strathdee, Robin E. Duncan
Publikováno v:
Biology, Vol 12, Iss 9, p 1238 (2023)
Barth syndrome (BTHS) is caused by mutations in tafazzin resulting in deficits in cardiolipin remodeling that alter major metabolic processes. The tafazzin gene is encoded on the X chromosome, and therefore BTHS primarily affects males. Female carrie
Externí odkaz:
https://doaj.org/article/a6816bbca01e4a64aa89ac936befd020