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Q36202800-CA4237C9-13E7-4752-9607-89475632EDAA
Q36202800-CA4237C9-13E7-4752-9607-89475632EDAA
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http://www.wikidata.org/entity/statement/Q36202800-CA4237C9-13E7-4752-9607-89475632EDAA
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.
P2860
Q36202800-CA4237C9-13E7-4752-9607-89475632EDAA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36202800-CA4237C9-13E7-4752-9607-89475632EDAA
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wasDerivedFrom
d490bb1d77b18bd9658bc543861bad7308e7cacf
P2860
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia