Order reprints

Open Access Highly Accessed

Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family

Obaid Ur Rahman, Nadeem Khawar, Muhammad Aman Khan, Jawad Ahmed, Kamran Khattak, Jumana Yousuf Al-Aama, Muhammad Naeem and Musharraf Jelani*

Diagnostic Pathology 2013, 8:78  doi:10.1186/1746-1596-8-78

This article is currently available as a provisional PDF. Reprints are produced from the final PDF, which is normally produced within 3 weeks.

Please complete the following form to register your interest in ordering reprints of this article. BioMed Central will contact you by email when the final PDF is available with details of how to obtain a quotation and place an order.

Fields marked * are required

http://www.diagnosticpathology.org/content/8/1/78
1746-1596-8-78