A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa-Reference-Cited by-同舟云学术

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A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa

Published:1994 Issue:10 Volume:3 Page:1909-1910
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Baudoin Christian,Miquel Corinne,Gagnoux-Palacios Laurent,Pulkkinen Leena,Christiano Angela M.,Uitto Jouni,Tadini Gianluca,Ortonne Jean-Paul,Meneguzzl Guerrino

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/10/1909/1880119/3-10-1909.pdf

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4. Skin Gene and Cell Therapy;Harper's Textbook of Pediatric Dermatology;2011-05-24

5. Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene;Journal of Investigative Dermatology;2006-08

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