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Q38669720-5708302E-2A6B-444B-8405-0BE0C79C208E
Q38669720-5708302E-2A6B-444B-8405-0BE0C79C208E
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Statement
http://www.wikidata.org/entity/statement/Q38669720-5708302E-2A6B-444B-8405-0BE0C79C208E
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
P2860
Q38669720-5708302E-2A6B-444B-8405-0BE0C79C208E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38669720-5708302E-2A6B-444B-8405-0BE0C79C208E
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type
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wasDerivedFrom
4e8126c2923da289cca696ea0a8d128c315d4b65
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.