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Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity

✍ Scribed by O. Messaoud; M. Ben Rekaya; H. Ouragini; S. Benfadhel; H. Azaiez; R. Kefi; N. Gouider-Khouja; I. Mokhtar; A. Amouri; M. S. Boubaker; M. Zghal; S. Abdelhak

Publisher: Springer-Verlag
Year: 2011
Tongue: English
Weight: 380 KB
Volume: 304
Category: Article
ISSN: 0340-3696
DOI: 10.1007/s00403-011-1190-4

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