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1
Q38940737-B08FD886-447F-4430-96B6-5493B0ED078B
Q38940737-B08FD886-447F-4430-96B6-5493B0ED078B
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Statement
http://www.wikidata.org/entity/statement/Q38940737-B08FD886-447F-4430-96B6-5493B0ED078B
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
P2860
Q38940737-B08FD886-447F-4430-96B6-5493B0ED078B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38940737-B08FD886-447F-4430-96B6-5493B0ED078B
rank
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type
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wasDerivedFrom
72e0c17f50f0ed58e2059f525f4cae0909489f68
P2860
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.