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Q49167995-CB5C6714-E686-4ADF-A823-3A3CDE3AB281
Q49167995-CB5C6714-E686-4ADF-A823-3A3CDE3AB281
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http://www.wikidata.org/entity/statement/Q49167995-CB5C6714-E686-4ADF-A823-3A3CDE3AB281
Global distribution of the most prevalent deletions causing hypotonia-cystinuria syndrome.
P2860
Q49167995-CB5C6714-E686-4ADF-A823-3A3CDE3AB281
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49167995-CB5C6714-E686-4ADF-A823-3A3CDE3AB281
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wasDerivedFrom
fc9d7ea8bd635f15a3e6703e931c25b9151c3b81
P2860
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.