Novel variant p.(Ala102Thr) in SDHB...

Annals of Human Genetics 2020 / 03

Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature

Kaur, Parneet, Sharma, Suvasini, Kadavigere, Rajagopal, Girisha, Katta Mohan, Shukla, Anju
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Journal:
Annals of Human Genetics
DOI:
10.1111/ahg.12377
Date:
March, 2020
File:
PDF, 819 KB
2020
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