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Q35000461-101CEF07-FC00-470A-AF82-23C980B0F798
Q35000461-101CEF07-FC00-470A-AF82-23C980B0F798
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35000461-101CEF07-FC00-470A-AF82-23C980B0F798
Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations.
P2860
Q35000461-101CEF07-FC00-470A-AF82-23C980B0F798
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35000461-101CEF07-FC00-470A-AF82-23C980B0F798
rank
NormalRank
type
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Statement
wasDerivedFrom
704cef1479d91a8cf5e114777ea1f2acf2bb949d
P2860
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).