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Q26998733-70AC57D0-279F-4917-9EE6-7BCCB3189500
Q26998733-70AC57D0-279F-4917-9EE6-7BCCB3189500
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26998733-70AC57D0-279F-4917-9EE6-7BCCB3189500
The National Institutes of Health undiagnosed diseases program
P2860
Q26998733-70AC57D0-279F-4917-9EE6-7BCCB3189500
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26998733-70AC57D0-279F-4917-9EE6-7BCCB3189500
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wasDerivedFrom
b75d60dd7f8369000e225f51fc02a240b6f235bf
P2860
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases