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Q42752301-21AE53AB-DA02-4D90-BB22-725171FB2305
Q42752301-21AE53AB-DA02-4D90-BB22-725171FB2305
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Statement
http://www.wikidata.org/entity/statement/Q42752301-21AE53AB-DA02-4D90-BB22-725171FB2305
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-21AE53AB-DA02-4D90-BB22-725171FB2305
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-21AE53AB-DA02-4D90-BB22-725171FB2305
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wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.