Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins

Journal article

Peer reviewed

Peter John, Muhammad Tariq, MUHAMMAD ARSHAD Rafiq, Muhammad AMIN-UD-DIN, Dost Muhammad, Ishrat Waheed, Muhammad Ansar and Wasim Ahmad

Archives of dermatological research (Print), Vol.298(3), pp.135-137

01/08/2006

PMID: 16770573

Abstract

Biological and medical sciences

Dermatology

Hair and nails disorders

Medical sciences

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Title: Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins
Creators - without role: Peter John - Quaid-i-Azam University
Muhammad Tariq - Quaid-i-Azam University
MUHAMMAD ARSHAD Rafiq - COMSATS University Islamabad
Muhammad AMIN-UD-DIN - Government College of Science
Dost Muhammad - Quaid-i-Azam University
Ishrat Waheed - Quaid-i-Azam University
Muhammad Ansar - COMSATS University Islamabad
Wasim Ahmad - Quaid-i-Azam University
Publication Details: Archives of dermatological research (Print), Vol.298(3), pp.135-137
Publisher: Springer
Identifiers: 9933829408331
Academic Unit: University of Tabuk
Language: English
Resource Type: Journal article