A novel mutation in LAMA3A gene in a child with laryngo-onycho-cutaneous syndrome from the Indian subcontinent-Reference-Cited by-同舟云学术

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A novel mutation in LAMA3A gene in a child with laryngo-onycho-cutaneous syndrome from the Indian subcontinent

Published:2020 Issue:5 Volume:86 Page:555
ISSN:0378-6323
Container-title:Indian Journal of Dermatology, Venereology and Leprology
language:en
Short-container-title:Indian J Dermatol Venereol Leprol

Author:

Ranugha PSS,Shastry Veeranna

Publisher

Scientific Scholar

Subject

Infectious Diseases,Dermatology

Reference7 articles.

1. McGrath JA. Genetic blistering diseases. In: Chalmers R, Barker J, Griffiths C, Bleiker T, Creamer D, editors. ROOK's Textbook of Dermatology. 9th ed. West Sussex, UK: John Wiley and Sons, Ltd.; 2016. p. 71.14.

2. Varki R, Sadowski S, Pfendner E, Uitto J. Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants.J Med Genet 2006;43:641-52.

Cited by 4 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. Conjunctiva;Ocular Pathology;2025

2. c.151dup variant in LAMA3 in Pakistani patients affected with Shabbir Syndrome but showing mild symptoms;Pakistan Journal of Medical Sciences;2023-05-16

3. The natural history of laryngo‐onycho‐cutaneous syndrome: A case series of six pediatric patients and literature review;Pediatric Dermatology;2021-09

4. Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A;Clinical and Experimental Dermatology;2021-02-18

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