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Q37370853-340199DA-CB41-4510-8174-925D9F5B50F6
Q37370853-340199DA-CB41-4510-8174-925D9F5B50F6
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http://www.wikidata.org/entity/statement/Q37370853-340199DA-CB41-4510-8174-925D9F5B50F6
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity
P2860
Q37370853-340199DA-CB41-4510-8174-925D9F5B50F6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37370853-340199DA-CB41-4510-8174-925D9F5B50F6
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dfdce7d4cb95be7eb69aa3bb9cd42f649756bb8b
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.