Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 1 (of 1 Records) |
Query Trace: Multiple Mitochondrial Dysfunctions Syndrome[original query] |
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Report of the Third Family with Multiple Mitochondrial Dysfunctions Syndrome 5 Caused by the Founder Variant p.(Glu87Lys) in ISCA1. Journal of pediatric genetics 2018 8 7 (3): 130-133. Shukla Anju, Kaur Parneet, Girisha Katta |
- Page last reviewed:Feb 1, 2024
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