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Q24299114-E62D32C0-B90F-435D-A105-553C59C343E1
Q24299114-E62D32C0-B90F-435D-A105-553C59C343E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299114-E62D32C0-B90F-435D-A105-553C59C343E1
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone
P2860
Q24299114-E62D32C0-B90F-435D-A105-553C59C343E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299114-E62D32C0-B90F-435D-A105-553C59C343E1
rank
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type
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Statement
wasDerivedFrom
797f2a54ad92a99665079b65017cafe49c5977df
P2860
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis