An investigation into theMMP1gene promoter region polymorphism - 1607 2G with recessive dystrophic epidermolysis bullosa disease severity in northeastern Mexican patients-Reference-Cited by-同舟云学术

An investigation into theMMP1gene promoter region polymorphism - 1607 2G with recessive dystrophic epidermolysis bullosa disease severity in northeastern Mexican patients

Published:2014-06-05 Issue:8 Volume:53 Page:985-990
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Garza-Gómez Jorge¹,Cerda-Flores Ricardo M.²,Gómez-Flores Minerva¹,Salas-Alanís Julio C.¹,Ocampo-Candiani Jorge¹,Martínez-Garza Laura E.³,South Andrew P.⁴,Gallardo-Blanco Hugo L.³

Affiliation:

1. Department of Dermatology; Universidad Autónoma de Nuevo León; Hospital Universitario “Jose E. González”; Monterrey Mexico

2. Facultad de Enfermería; Universidad Autónoma de Nuevo León; Monterrey Mexico

3. Department of Genetics; Universidad Autónoma de Nuevo León; Hospital Universitario “José E. González”; Monterrey Mexico

4. Division of Cancer Research; Medical Research Institute; Ninewells Hospital and Medical School; University of Dundee; Dundee UK

Publisher

Wiley

Subject

Dermatology

Reference31 articles.

1. The classification of inherited epidermolysis bullosa (EB): report of the third international consensus meeting on diagnosis and classification of EB;Fine;J Am Acad Dermatol,2008

2. Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type VII collagen gene;Gardella;Br J Dermatol,2002