Identification of a Homozygous One-Basepair Deletion in Exon 14 of the LAMB3 in a Patient with Herlitz Junctional Epidermolysis Bullosa and Prenatal Diagnosis in a Family at Risk for Recurrence-Reference-Cited by-同舟云学术

Identification of a Homozygous One-Basepair Deletion in Exon 14 of the LAMB3 in a Patient with Herlitz Junctional Epidermolysis Bullosa and Prenatal Diagnosis in a Family at Risk for Recurrence

Published:1995-04 Issue:4 Volume:104 Page:462-466
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Vailly Joëlle,Pulkkinen Leena,Miquel Corinne,Christiano Angela M.,Gerecke Donald,Burgeson Robert E.,Uitto Jouni,Ortonne Jean-Paul,Meneguzzi Guerrino

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference32 articles.

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4. Desmosomes and hemidesmoses: constitutive molecular components;Schwartz;Annu Rev Cell Biol,1990

5. Clinicopathologic types of epidermolysis bullosa and their nondermatologic complications;Pearson;Arch Dermatol,1998

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