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Q28248837-34DB179B-6014-4CB9-8B7C-027A730D9FE5
Q28248837-34DB179B-6014-4CB9-8B7C-027A730D9FE5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28248837-34DB179B-6014-4CB9-8B7C-027A730D9FE5
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
P2860
Q28248837-34DB179B-6014-4CB9-8B7C-027A730D9FE5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28248837-34DB179B-6014-4CB9-8B7C-027A730D9FE5
rank
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type
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Statement
wasDerivedFrom
5f6c78647f477a1ef31bca6997d646e21616603e
P2860
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)