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Q37185993-310C44E7-F2C7-45FC-A959-2B8C506E02FB
Q37185993-310C44E7-F2C7-45FC-A959-2B8C506E02FB
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http://www.wikidata.org/entity/statement/Q37185993-310C44E7-F2C7-45FC-A959-2B8C506E02FB
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
P2860
Q37185993-310C44E7-F2C7-45FC-A959-2B8C506E02FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37185993-310C44E7-F2C7-45FC-A959-2B8C506E02FB
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8555ed94f66d5ab508631223a31e0c45b389d00d
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.