Novel ENU-induced eye mutations in the mouse: models for human eye disease

By Brown S.D.M.  

Human Molecular Genetics, Vol. 11, Iss. 7, 2002-04 ,pp. : 755-767

Oxford University Press

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

By 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.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1230-1247

Oxford University Press

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A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)

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Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 1069-1074

Oxford University Press

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Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

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Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1673-1677

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A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3

By Mendoza Gustavo   Pemberton Trevor   Lee Kwanghyuk   Scarel-Caminaga Raquel   Mehrian-Shai Ruty   Gonzalez-Quevedo Catalina   Ninis Vasiliki   Hartiala Jaana   Allayee Hooman   Snead Malcolm   Leal Suzanne   Line Sergio   Patel Pragna  

Human Genetics, Vol. 120, Iss. 5, 2007-01 ,pp. : 653-662

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