Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11

Published 2018 View Full Article

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Title
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11
Authors
Keywords
NDUFB11, Mitochondrial complex I deficiency, Histiocytoid cardiomyopathy, Congenital sideroblastic anemia
Journal
European Journal of Medical Genetics
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2018-11-11
DOI
10.1016/j.ejmg.2018.11.006

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