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Q24568013-0DE6C586-3B33-4E15-A049-E434B6CEE431
Q24568013-0DE6C586-3B33-4E15-A049-E434B6CEE431
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http://www.wikidata.org/entity/statement/Q24568013-0DE6C586-3B33-4E15-A049-E434B6CEE431
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta
P2860
Q24568013-0DE6C586-3B33-4E15-A049-E434B6CEE431
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24568013-0DE6C586-3B33-4E15-A049-E434B6CEE431
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wasDerivedFrom
6083386828452fa8426acedb6f3cea508db7e4b7
P2860
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.