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.
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Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth AgenesisAssociations Between TGFA/TGFB3/MSX1 Gene Polymorphisms and Congenital Non-Syndromic Hearing Impairment in a Chinese Population.MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathwayUnusual report of non-syndromic permanent unilateral mandibular canine agenesis
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.
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2015 nî lūn-bûn
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2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
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2015年论文
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name
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@ast
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@en
type
label
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@ast
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@en
prefLabel
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@ast
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@en
P2093
P2860
P1433
P1476
An aberrant splice acceptor si ...... agenesis in a Japanese family.
@en
P2093
Akio Shibata
Atsuo Nakayama
Hiroki Goto
Hitoshi Miyachi
Junichiro Machida
Kazuo Shimozato
Masashi Kimura
Mitsuko Nakashima
Naomichi Matsumoto
Seishi Yamaguchi
P2860
P304
P356
10.1371/JOURNAL.PONE.0128227
P407
P577
2015-06-01T00:00:00Z