Vitiligo and melanocytic nevi: New findings in Coffin-Siris syndrome associated with ARID1 germline mutation
Author:
Funder
National Cancer Institute
National Institutes of Health
Publisher
Elsevier BV
Subject
Dermatology
Reference10 articles.
1. Coffin Siris syndrome: a disorder of SWI|/SNF pathway;Mishra;Genet Clin,2016
2. Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome;Tsurusaki;Nat Genet,2012
3. The ARID1B phenotype: what we have learned so far;Santen;Am J Med Genet C Semin Med Genet,2014
4. Report of a patient with a constitutional missense mutation in SMARCB1, Coffin–Siris phenotype, and schwannomatosis;Gossai;Am J Med Genet A,2015
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Pigmentation abnormalities in Coffin‐Siris syndrome;Clinical Genetics;2023-05-11
2. Early Malignant Melanoma Detection, Especially in Persons with Pigmented Skin;Advances in Skin & Wound Care;2023-02
3. Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report;BMC Pediatrics;2022-08-13
4. Genodermatoses associated with melanocytic nevi;Clinics in Dermatology;2022-07
5. Koebner phenomenon of vitiligo associated with Coffin-Siris syndrome;European Journal of Dermatology;2020-06
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