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Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans

Hanan E. Shamseldin; Laura L. Smith; Amal Kentab; Hisham Alkhalidi; Brady Summers; Haifa Alsedairy; Yong Xiong; Vandana A. Gupta; Fowzan S. Alkuraya
Human Genetics · Vol. 135, Issue 1 · pp. 21-30 · 2016
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2016-01-01
Publication Year2016
Volume135
Issue1
Pages21-30
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-015-1608-8

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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