Novel Homozygous Variant in TTC19 Causing Mitochondrial...

Seminars in Pediatric Neurology 2018 / 07 Vol. 26

Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype

Conboy, Erin, Selcen, Duygu, Brodsky, Michael, Gavrilova, Ralitza, Lan Ho, Mai
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Volume:
26
Language:
english
Journal:
Seminars in Pediatric Neurology
DOI:
10.1016/j.spen.2018.04.003
Date:
July, 2018
File:
PDF, 452 KB
english, 2018
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