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Q24533422-9A50D08B-6996-44CA-AF40-B0D35D97C86B
Q24533422-9A50D08B-6996-44CA-AF40-B0D35D97C86B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-9A50D08B-6996-44CA-AF40-B0D35D97C86B
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P2860
Q24533422-9A50D08B-6996-44CA-AF40-B0D35D97C86B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-9A50D08B-6996-44CA-AF40-B0D35D97C86B
rank
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Statement
wasDerivedFrom
7b58157747859b308c6995fe688aa24475c66bbf
P2860
Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1.