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Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta

BACKGROUND: Amelogenesis imperfecta (AI) is an inherited disorder characterized by abnormal formation of tooth enamel. Although several genes responsible for AI have been reported, not all causative genes for human AI have been identified to date. AMI rat has been reported as an autosomal recessive...

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Autori principali: Muto, Taro, Miyoshi, Keiko, Horiguchi, Taigo, Hagita, Hiroko, Noma, Takafumi
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3464675/
https://ncbi.nlm.nih.gov/pubmed/22676574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-7-34
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