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Q33903384-8A9F02EE-116B-46C0-9610-F17837942BF6
Q33903384-8A9F02EE-116B-46C0-9610-F17837942BF6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33903384-8A9F02EE-116B-46C0-9610-F17837942BF6
The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases.
P2860
Q33903384-8A9F02EE-116B-46C0-9610-F17837942BF6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33903384-8A9F02EE-116B-46C0-9610-F17837942BF6
rank
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Statement
wasDerivedFrom
1375eff73ae03b8eb4b9cf03f4fac7c45d85746d
P2860
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.