A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta-Reference-Cited by-同舟云学术

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta

Published:2010-01-12 Issue:7 Volume:19 Page:1230-1247
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Barron Martin J.,Brookes Steven J.,Kirkham Jennifer,Shore Roger C.,Hunt Charlotte,Mironov Aleksandr,Kingswell Nicola J.,Maycock Joanne,Shuttleworth C. Adrian,Dixon Michael J.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference44 articles.

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3. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification;J. Oral Pathol.,1988

5. Enamel formation and amelogenesis imperfecta;Cells Tissues Organs,2007

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