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Q37138441-0257A976-728B-4BB1-ADD7-29F56845E4ED
Q37138441-0257A976-728B-4BB1-ADD7-29F56845E4ED
BestRank
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http://www.wikidata.org/entity/statement/Q37138441-0257A976-728B-4BB1-ADD7-29F56845E4ED
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.
P2860
Q37138441-0257A976-728B-4BB1-ADD7-29F56845E4ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37138441-0257A976-728B-4BB1-ADD7-29F56845E4ED
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wasDerivedFrom
ddc30ac34d8641467c2a612e25853eac7cd55b49
P2860
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement