Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed.

In order to identify the gene for human X-linked anhidrotic ectodermal dysplasia (EDA), a translocation breakpoint in a female with t(X;1)(q13.1;p36.3) and EDA (patient AK) was finely mapped. The EDA region contains five groups of rare-cutter restriction sites that define CpG islands. The two more c...

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Detalhes bibliográficos
Main Authors: Srivastava, A. K., Montonen, O., Saarialho-Kere, U., Chen, E., Baybayan, P., Pispa, J., Limon, J., Schlessinger, D., Kere, J.
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1914968/
https://ncbi.nlm.nih.gov/pubmed/8554048
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