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Q34478269-E86413A4-BB83-4E46-A430-FF53E7B75D34
Q34478269-E86413A4-BB83-4E46-A430-FF53E7B75D34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478269-E86413A4-BB83-4E46-A430-FF53E7B75D34
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.
P2860
Q34478269-E86413A4-BB83-4E46-A430-FF53E7B75D34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478269-E86413A4-BB83-4E46-A430-FF53E7B75D34
rank
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type
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Statement
wasDerivedFrom
1ca83383762783fbcf6bb4eef25784bf0f586a94
P2860
Insights into the PX (phox-homology) domain and SNX (sorting nexin) protein families: structures, functions and roles in disease.