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Q24310078-96D060AC-EAFD-4C72-A6AE-CA38B0CA7BE6
Q24310078-96D060AC-EAFD-4C72-A6AE-CA38B0CA7BE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310078-96D060AC-EAFD-4C72-A6AE-CA38B0CA7BE6
Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins
P2860
Q24310078-96D060AC-EAFD-4C72-A6AE-CA38B0CA7BE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310078-96D060AC-EAFD-4C72-A6AE-CA38B0CA7BE6
rank
NormalRank
type
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Statement
wasDerivedFrom
4c6d20bbaa6d1f6c836e945694ec0d2fbad0c4b4
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis