Exclusion of COL7A1 mutation in Kindler syndrome
- 1 March 2002
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 46 (3) , 447-450
- https://doi.org/10.1067/mjd.2002.117523
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 8 references indexed in Scilit:
- Kindler syndrome: absence of definite ultrastructural feature.Journal of the American Academy of Dermatology, 1999
- Abnormal deposition of type VII collagen in Kindler syndrome.Archives of Dermatological Research, 1999
- Immunohistochemical, Ultrastructural, and Molecular Features of Kindler Syndrome Distinguish It From Dystrophic Epidermolysis BullosaArchives of Dermatology, 1997
- Strategy for identification of sequence variants in COL7A1 and a novel 2-bp deletion mutation in recessive dystrophic epidermolysis bullosaHuman Mutation, 1997
- Kindler SyndromeArchives of Dermatology, 1996
- Poikiloderma of Theresa Kindler: Report of a Case with Ultrastrectural Study, and Review of the LiteraturePediatric Dermatology, 1989
- Kindler Syndrome: Report of Two Cases and Review of the LiteraturePediatric Dermatology, 1989
- CONGENITAL POIKILODERMA WITH TRAUMATIC BULLA FOKMATION AND PROGRESSIVE CUTANEOUS ATROPHY.British Journal of Dermatology, 1954