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Q59136971-3C88CD07-7195-4323-99E6-8CCEB9637739
Q59136971-3C88CD07-7195-4323-99E6-8CCEB9637739
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http://www.wikidata.org/entity/statement/Q59136971-3C88CD07-7195-4323-99E6-8CCEB9637739
Missense variants in in a patient with Joubert syndrome
P2860
Q59136971-3C88CD07-7195-4323-99E6-8CCEB9637739
BestRank
Statement
http://www.wikidata.org/entity/statement/Q59136971-3C88CD07-7195-4323-99E6-8CCEB9637739
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wasDerivedFrom
5bc21aa48e7a129de474676a2638e9f64383e257
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.