A mutation in the LAMC2 gene causes the Herlitz junctional epidermolysis bullosa (H-JEB) in two French draft horse breeds

Epidermolysis bullosa (EB) is a heterogeneous group of inherited diseases characterised by skin blistering and fragility. In humans, one of the most severe forms of EB known as Herlitz-junctional EB (H-JEB), is caused by mutations in the laminin 5 genes. EB has been described in several species, lik...

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Detalles Bibliográficos
Autores principales: Milenkovic, Dragan, Chaffaux, Stéphane, Taourit, Sead, Guérin, Gérard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732698/
https://www.ncbi.nlm.nih.gov/pubmed/12633536
http://dx.doi.org/10.1186/1297-9686-35-2-249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732698/
https://www.ncbi.nlm.nih.gov/pubmed/12633536
http://dx.doi.org/10.1186/1297-9686-35-2-249

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