Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome-Reference-Cited by-同舟云学术

Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome

Published:2004-01 Issue:1 Volume:122 Page:78-83
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Ashton Gabrielle H.S.,Irwin Mclean W.H.,South Andrew P.,Oyama Noritaka,Smith Frances J.D.,Al-Suwaid Raouf,Al Ismaily Abla,Atherton David J.,Harwood Catherine A.,Leigh Irene M.,Moss Celia,Didona Biagio,Zambruno Giovanna,Patrizi Annalisa,Eady Robin A.J.,Mcgrath John A.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference19 articles.

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4. Revised classification system for inherited epidermolysis bullosa. Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa;Fine;J Am Acad Dermatol,2000

5. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes;Ganguly;Proc Natl Acad Sci USA,1993

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