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d356777109e8c8052d56cf9a0d8b459d14aff4a9
d356777109e8c8052d56cf9a0d8b459d14aff4a9
Reference
http://www.wikidata.org/reference/d356777109e8c8052d56cf9a0d8b459d14aff4a9
Q1101694-30917362-CFF0-4E94-B7BF-55ADC430AAF3
Q1101694-88DDF85A-9204-4A69-9D46-EF7FF3A22EF1
Q1101694-9C18B73F-788A-4124-B450-67409057E05D
wasDerivedFrom
d356777109e8c8052d56cf9a0d8b459d14aff4a9
Reference
http://www.wikidata.org/reference/d356777109e8c8052d56cf9a0d8b459d14aff4a9
type
Reference
P248
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.