Associated Papers
Novel variants in LAMA3 and COL7A1 and recurrent variant in KRT5 underlying epidermolysis bullosa in five Chinese families.
Wang R et al.
Frontiers of Medicine, 2022
The natural history of laryngo-onycho-cutaneous syndrome: A case series of six pediatric patients and literature review.
Prodinger C et al.
Pediatric Dermatology, 2021
Application of whole exome sequencing in elucidating the phenotype and genotype spectrum of junctional epidermolysis bullosa: A preliminary experience of a tertiary care centre in India.
Yenamandra VK et al.
Journal of Dermatological Science, 2017
c.151dup variant in LAMA3 in Pakistani patients affected with Shabbir Syndrome but showing mild symptoms.
Ullah A et al.
Pakistan Journal of Medical Sciences, 0
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