Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome.
Wang S, Yazawa E, Keating EM, Mazumdar N, Hauschild A, Ma Q, Wu H, Xu Y, Shi X, Strathdee D, Gerszten RE, Schlame M, Pu WT.
Wang S, et al. Among authors: schlame m.
Hum Mol Genet. 2023 Jun 5;32(12):2055-2067. doi: 10.1093/hmg/ddad041.
Hum Mol Genet. 2023.
PMID: 36917259
Free PMC article.