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Q36814753-1F29DF21-1DC9-4260-BE74-5F3C32D140FB
Q36814753-1F29DF21-1DC9-4260-BE74-5F3C32D140FB
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Statement
http://www.wikidata.org/entity/statement/Q36814753-1F29DF21-1DC9-4260-BE74-5F3C32D140FB
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function
P2860
Q36814753-1F29DF21-1DC9-4260-BE74-5F3C32D140FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36814753-1F29DF21-1DC9-4260-BE74-5F3C32D140FB
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wasDerivedFrom
504362a53c47d6e3030f8c520f6a1583716a3431
P2860
The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation.