Naxos disease in an Arab family is not caused by the Pk2157del2 mutation. Evidence for exclusion of the plakoglobin gene

Manfred Stuhrmann; Iqbal A. Bukhari; El-Harith A. El-Harith

Article Information

vol. 25 no. 10 1449-1452

PubMed

15494820

Published By

Saudi Medical Journal

Online ISSN

1658-3175

History

Published online January 8, 2021.

Copyright: © Saudi Medical Journal This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Author Information

Manfred Stuhrmann,
Iqbal A. Bukhari and
El-Harith A. El-Harith

Institute of Human Genetics, Medical University Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Federal Republic of Germany. Tel. +49 (511) 5323719. Fax. +49 (511) 5325865. E-mail: stuhrmann.manfred{at}mh-hannover.de
Department of Dermatology, King Fahad Hospital of the University, King Faisal University, Al-Khobar, Kingdom of Saudi Arabia.
Institute of Human Genetics, Medical University Hannover, Hannover, Federal Republic of Germany.