Identification of a nonsence mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

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Published in:Human genetics 1992, Vol.90 (4), p.413-416
Main Authors: ALDRED, M. J, CRAWFORD, P. J. M, ROBERTS, E, THOMAS, N. S. T
Format: Article
Language:English
Subjects:
Biological and medical sciences
Facial bones, jaws, teeth, parodontium: diseases, semeiology
Medical sciences
Non tumoral diseases
Otorhinolaryngology. Stomatology
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container_end_page 416
container_issue 4
container_start_page 413
container_title Human genetics
container_volume 90
creator ALDRED, M. J
CRAWFORD, P. J. M
ROBERTS, E
THOMAS, N. S. T
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ispartof Human genetics, 1992, Vol.90 (4), p.413-416
issn 0340-6717
1432-1203
language eng
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source Springer Online Journal Archives
subjects Biological and medical sciences
Facial bones, jaws, teeth, parodontium: diseases, semeiology
Medical sciences
Non tumoral diseases
Otorhinolaryngology. Stomatology
title Identification of a nonsence mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)
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