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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Detalles Bibliográficos
Autores principales: Muto, Taro, Miyoshi, Keiko, Horiguchi, Taigo, Hagita, Hiroko, Noma, Takafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464675/
https://www.ncbi.nlm.nih.gov/pubmed/22676574
http://dx.doi.org/10.1186/1750-1172-7-34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464675/
https://www.ncbi.nlm.nih.gov/pubmed/22676574
http://dx.doi.org/10.1186/1750-1172-7-34

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