Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients
Author:
Affiliation:
1. Department of Dermatology; Gunma University Graduate School of Medicine; Maebashi Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14623/fullpdf
Reference9 articles.
1. Familial acanthosis nigricans due to K650T FGFR3 mutation;Berk;Arch Dermatol,2007
2. A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene;Tavormina;Am J Hum Genet,1999
3. FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease;Ornitz;Genes Dev,2002
4. Altered FGF signalling in congenital craniofacial and skeletal disorders;Moosa;Semin Cell Dev Biol,2016
5. Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene;Leroy;Am J Med Genet A,2007
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2. Familial isolated acanthosis nigricans as a result of a recurrent FGFR3 truncating mutation;Clinical and Experimental Dermatology;2023-02-27
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5. Autosomal dominant familial acanthosis nigricans caused by a C-terminal nonsense mutation of FGFR3;Journal of Human Genetics;2021-02-12
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