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Q28115318-4E75D8C9-AED0-42FF-955B-8537D9C89FE4
Q28115318-4E75D8C9-AED0-42FF-955B-8537D9C89FE4
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http://www.wikidata.org/entity/statement/Q28115318-4E75D8C9-AED0-42FF-955B-8537D9C89FE4
Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis
P2860
Q28115318-4E75D8C9-AED0-42FF-955B-8537D9C89FE4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28115318-4E75D8C9-AED0-42FF-955B-8537D9C89FE4
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wasDerivedFrom
36e9c72aed2a7e7e12f941fb26ca1775273b826f
P2860
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.