Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia-Reference-Cited by-同舟云学术

Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia

Published:2015-11-26 Issue:2 Volume:174 Page:439-443
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Jerbi M.¹,Ben Rekaya M.¹,Naouali C.¹,Jones M.¹²,Messaoud O.¹,Tounsi H.³,Nagara M.¹,Chargui M.¹,Kefi R.¹,Boussen H.⁴,Mokni M.⁵⁶,Mrad R.⁷,Boubaker M.S.³,Abdelhak S.²,Khaled A.²,Zghal M.²,Yacoub-Youssef H.¹

Affiliation:

1. Laboratoire de Génomique Biomédicale et Oncogénétique; Institut Pasteur de Tunis; Université Tunis El Manar; Tunis Tunisie

2. Service de Dermatologie; Hôpital Charles Nicolle; Tunis Tunisie

3. Laboratoire d'Anatomie Pathologique Humaine et Expérimentale; Institut Pasteur de Tunis; Université Tunis El Manar; Tunis Tunisie

4. Service d'Oncologie Médicale; Hôpital Abderrahman Mami; Ariana Tunisie

5. Unité de Recherche ‘Troubles Héréditaires de la Kératinisation’ UR 24/04; Hôpital La Rabta; Tunis Tunisie

6. Service de Dermatologie; Hôpital La Rabta; Tunis Tunisie

7. Service de Génétique; Hôpital Charles Nicolle; Tunis Tunisie

Funder

Tunisian Ministry of Public Health

Tunisian Ministry of Higher Education

Laboratory of Biomedical Genomics and Oncogenetics

Projet Collaboratif Interne PCI-Melanoma, IPT

Seventh Framework Programme

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.14046/fullpdf

Reference15 articles.

1. Defective repair replication of DNA in xeroderma pigmentosum;Cleaver;Nature,1968

2. A new XPC gene splicing mutation has lead to the highest worldwide prevalence of xeroderma pigmentosum in black Mahori patients;Cartault;DNA Repair (Amst),2011

3. Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 49 Tunisian cases;Zghal;Tunis Med,2005

4. Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity;Cleaver;Nat Rev Genet,2009

5. Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations;Schafer;Exp Dermatol,2013

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