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Q34054602-0F1D8232-5220-4130-BE63-E50573D8892A
Q34054602-0F1D8232-5220-4130-BE63-E50573D8892A
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http://www.wikidata.org/entity/statement/Q34054602-0F1D8232-5220-4130-BE63-E50573D8892A
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.
P2860
Q34054602-0F1D8232-5220-4130-BE63-E50573D8892A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34054602-0F1D8232-5220-4130-BE63-E50573D8892A
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wasDerivedFrom
d1a58bbf39d73863d31243152eab47f3901d9c8c
P2860
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement