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Q24532051-6795F369-510E-4E9C-A46E-AC1A96736EB8
Q24532051-6795F369-510E-4E9C-A46E-AC1A96736EB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532051-6795F369-510E-4E9C-A46E-AC1A96736EB8
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport
P2860
Q24532051-6795F369-510E-4E9C-A46E-AC1A96736EB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532051-6795F369-510E-4E9C-A46E-AC1A96736EB8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ad5e194e33d8b7d2d74428bd0aad80c5762ac098
P2860
Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor