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Q37364346-2AE547EE-0D3E-4AA9-913E-ABFEAF419054
Q37364346-2AE547EE-0D3E-4AA9-913E-ABFEAF419054
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37364346-2AE547EE-0D3E-4AA9-913E-ABFEAF419054
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.
P31
Q37364346-2AE547EE-0D3E-4AA9-913E-ABFEAF419054
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37364346-2AE547EE-0D3E-4AA9-913E-ABFEAF419054
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type
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wasDerivedFrom
bd90759b4b5d4de3f19ebc9f960f0b221a1ef9bc
P31
scholarly article