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Q36578717-02963C61-975E-45DC-BB94-CCB79EA4BB79
Q36578717-02963C61-975E-45DC-BB94-CCB79EA4BB79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36578717-02963C61-975E-45DC-BB94-CCB79EA4BB79
Common mechanisms in development and disease: BMP signaling in craniofacial development.
P2860
Q36578717-02963C61-975E-45DC-BB94-CCB79EA4BB79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36578717-02963C61-975E-45DC-BB94-CCB79EA4BB79
rank
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wasDerivedFrom
533f2ce4c21408419e7fa45cefd24646975d6063
P2860
A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).