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2
Q49174285-281FCBFE-DEC1-4F83-8A3D-467D3F8D8FB2
Q49174285-281FCBFE-DEC1-4F83-8A3D-467D3F8D8FB2
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Statement
http://www.wikidata.org/entity/statement/Q49174285-281FCBFE-DEC1-4F83-8A3D-467D3F8D8FB2
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
P2860
Q49174285-281FCBFE-DEC1-4F83-8A3D-467D3F8D8FB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49174285-281FCBFE-DEC1-4F83-8A3D-467D3F8D8FB2
rank
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type
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Statement
wasDerivedFrom
64db083ac64dce3f65e2c99cd1c5dd1cd753f52f
P2860
Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome.