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Expanding the clinical spectrum of mitochondrial 3‐hydroxy‐..:
Kılıç, Mustafa
;
Dorum, Sevil
;
Topak, Ali
...
American Journal of Medical Genetics Part A. 182 (2020) 7 - p. 1608-1614 , 2020
Link:
https://doi.org/10.1002/ajmg.a.61590
RT Journal T1 <Title>Expanding the clinical spectrum of mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.61590&Exemplar=1&LAN=DE A1 Kılıç, Mustafa A1 Dorum, Sevil A1 Topak, Ali A1 Yazıcı, Mutlu U. A1 Ezgu, Fatih S. A1 Coskun, Turgay PB Wiley YR 2020 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 182 IS 7 SP 1608 OP 1614 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.61590 DO https://doi.org/10.1002/ajmg.a.61590 SF ELIB - SuUB Bremen
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