X-Linked Anhidrotic (Hypohidrotic) Ectodermal Dysplasia Caused by a Novel Mutation in EDA1 Gene: 406T>G (Leu55Arg)
- 1 August 1999
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 113 (2) , 285-286
- https://doi.org/10.1046/j.1523-1747.1999.00656.x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.Journal of Medical Genetics, 1998
- Familial Skewed X Inactivation: A Molecular Trait Associated with High Spontaneous-Abortion Rate Maps to Xq28American Journal of Human Genetics, 1997
- X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinNature Genetics, 1996
- Ectodermal dysplasias: A clinical classification and a causal reviewAmerican Journal of Medical Genetics, 1994