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Q37472322-51658CD7-1092-4353-B543-28B4EE892A78
Q37472322-51658CD7-1092-4353-B543-28B4EE892A78
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http://www.wikidata.org/entity/statement/Q37472322-51658CD7-1092-4353-B543-28B4EE892A78
A developmental and genetic classification for midbrain-hindbrain malformations.
P2860
Q37472322-51658CD7-1092-4353-B543-28B4EE892A78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37472322-51658CD7-1092-4353-B543-28B4EE892A78
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wasDerivedFrom
d2a2bb0483b4723412b7389e66315ce863cb6552
P2860
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.