Carrier frequency of the recurrent mutation c.1643_1644delTG in the XPC gene and birth prevalence of the xeroderma pigmentosum in Morocco
Author:
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2011.01453.x/fullpdf
Reference9 articles.
1. Incidence of DNA repair deficiency disorders in western Europe: xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy;Kleijer;DNA Repair (Amst),2008
2. Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population;Hirai;Mutat Res,2006
3. A prevalent mutation with founder effect in xeroderma pigmentosum group C from North Africa;Soufir;J Invest Dermatol,2010
4. Systems of mating;Wright;Genetics,1921
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1. Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients;Egyptian Journal of Medical Human Genetics;2022-11-21
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