Lipoid proteinosis: A clinical and molecular study in Egyptian patients
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference33 articles.
1. A novel splice-site ECM1 gene mutation in a Lebanese girl with lipoid proteinosis;Abbas;Int. J. Dermatol.,2013
2. Novel mutations in extracellular matrix protein 1 gene in a Chinese patient with lipoid proteinosis;Bai;Chin. Med. J.,2016
3. Two Egyptian cases of lipoid proteinosis successfully treated with acitretin;Bakry;J. Dermatol. Case Rep.,2014
4. The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1;Chan;Exp. Dermatol.,2007
5. Lipoid proteinosis presenting with an unusual nonsense Q32X mutation in exon 2 of the extracellular matrix protein 1 gene;Chelvan;Australas. J. Dermatol.,2012
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3. Lipoid Proteinosis: Identification of a Novel Nonsense Mutation c.1246C>T:p.R416X in ECM1 gene from Bangladesh;Pakistan Journal of Medical Sciences;2023-05-16
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5. Lipoid proteinosis;Mucosa;2021-06-30
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