Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor gene
Author:
Affiliation:
1. Department of Biotechnology; Quaid-i-Azam University; Islamabad 45320 Pakistan
2. Institute of Human Genetics; University of Bonn; 53127 Bonn Germany
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.12293/fullpdf
Reference9 articles.
1. Familial acanthosis nigricans due to K650T FGFR3 mutation;Berk;Arch Dermatol,2007
2. Genes, growth factors and acanthosis nigricans;Torley;Br J Dermatol,2002
3. Benign acanthosis nigricans;Curth;Arch Dermatol,1967
4. Familial acanthosis nigricans;Dhar;Int J Dermatol,1996
5. Genetic studies on acanthosis nigricans;Curth;Arch Dermatol,1952
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4. Acanthosis nigricans in childhood: A cutaneous marker that should not be underestimated, especially in obese children;Acta Paediatrica;2019-10-14
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