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https://www.ias.ac.in/article/fulltext/jgen/090/03/0483-0487

xeroderma pigmentosum-V; late-onset phenotype; novel mutation; phenotype–genotype correlation.

Mariem Ben Rekaya¹ Olfa Messaoud¹ Amel Mebazaa^{2 3} Olfa Riahi^{2 3} Hela Azaiez¹ Rim Kefi¹ Mohamed Zghal⁴ Samir Boubaker⁵ Ahlem Amouri¹ Amel Ben Osman-Dhahri³ Sonia Abdelhak¹ Mourad Mokni^{2 3}

1. Molecular Investigation of Genetic Orphan Diseases Research Unit, Pasteur Institute of Tunis, 13 Place Pasteur, BP 74, 1002 Tunis Belvédère, Tunisia
2. Study of Hereditary Keratinization Disorders Research Unit, La Rabta Hospital of Tunis, La Rabta, 1007 Tunis, Tunisia
3. Dermatology Department, La Rabta Hospital of Tunis, La Rabta, 1007 Tunis, Tunisia
4. Dermatology Department, Habib Thameur Hospital, 1008 Tunis, Tunisia
5. Anatomo-Pathology Department, Pasteur Institute of Tunis, 13 Place Pasteur, BP 74, 1002 Tunis Belvédère, Tunisia

Published

December 2011

Manuscript received

2 March 2011

Manuscript revised

25 May 2011

Accepted

14 June 2011

Early published

14 November 2011