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Q41226986-FF7DCC40-3888-4CBE-9780-2AA49F421A80
Q41226986-FF7DCC40-3888-4CBE-9780-2AA49F421A80
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41226986-FF7DCC40-3888-4CBE-9780-2AA49F421A80
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
P2860
Q41226986-FF7DCC40-3888-4CBE-9780-2AA49F421A80
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41226986-FF7DCC40-3888-4CBE-9780-2AA49F421A80
rank
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type
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wasDerivedFrom
cc1ff51bbe1c6b2e015207cf9ba6ec07d914ce08
P2860
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects