Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis-Reference-Cited by-同舟云学术

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Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

Published:2013-01-24 Issue:4 Volume:50 Page:246-254
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Soler Vincent José,Tran-Viet Khanh-Nhat,Galiacy Stéphane D,Limviphuvadh Vachiranee,Klemm Thomas Patrick,St Germain Elizabeth,Fournié Pierre R,Guillaud Céline,Maurer-Stroh Sebastian,Hawthorne Felicia,Suarez Cyrielle,Kantelip Bernadette,Afshari Natalie A,Creveaux Isabelle,Luo Xiaoyan,Meng Weihua,Calvas Patrick,Cassagne Myriam,Arné Jean-Louis,Rozen Steven G,Malecaze François,Young Terri L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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4. NLRP1‐associated autoinflammatory disease with epithelial dyskeratosis;Pediatric Dermatology;2023-12-03

5. Role of the NLRP1 inflammasome in skin cancer and inflammatory skin diseases;British Journal of Dermatology;2023-10-27

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