Phenotype–genotype correlations for clinical variants caused by CYLD mutations

Author:

Nagy Nikoletta,Farkas Katalin,Kemény Lajos,Széll Márta

Funder

European Union and the State of Hungary

European Social Fund

Hungarian Scientific Research Fund

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference71 articles.

1. Five new CYLD mutations in skin appendage tumors and evidence that aspartic acid 681 in CYLD is essential for deubiquitinase activity;Almeida;J Invest Dermatol,2008

2. Skin adnexal neoplasms–part 1: an approach to tumours of the pilosebaceous unit;Alsaad;J Clin Pathol,2007

3. Multiple trichoepitheliomas – a novel mutation in the CYLD gene;Amaro;J Eur Acad Dermatol Venereol,2010

4. History of a remarkable case of tumours, developed on the head and face; accompanied with a similar disease in the abdomen;Ancell;Med Chir Trans,1842

5. The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas;Biggs;Oncogene,1996

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