Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity.

ABSTRACT:

SUBMITTER: Berhe S 

PROVIDER: S-EPMC6269299 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature