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Q37364346-9FB97F1C-26A4-4F7D-8512-E6F57C65F296
Q37364346-9FB97F1C-26A4-4F7D-8512-E6F57C65F296
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37364346-9FB97F1C-26A4-4F7D-8512-E6F57C65F296
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.
P698
Q37364346-9FB97F1C-26A4-4F7D-8512-E6F57C65F296
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37364346-9FB97F1C-26A4-4F7D-8512-E6F57C65F296
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
bd90759b4b5d4de3f19ebc9f960f0b221a1ef9bc
P698
18565097
http://www.w3.org/2001/XMLSchema#string