Associated Papers
Case Report: Alpha6 Integrin Disorder Presenting in Childhood with Nail Dysplasia and Onycholysis But No History of Fragile or Bullous Skin Changes.
Zalesny AN et al.
Global Medical Genetics, 2024
Very-Early-Onset Inflammatory Bowel Disease in a Patient With Junctional Epidermolysis Bullosa With a Homozygous Mutation in the α6 Integrin Gene (ITGA6).
Vahidnezhad H et al.
Inflammatory Bowel Diseases, 2021
Compound heterozygosity for novel splice site mutations of ITGA6 in lethal junctional epidermolysis bullosa with pyloric atresia.
Masunaga T et al.
The Journal of Dermatology, 2017
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations.
Schumann H et al.
The British Journal of Dermatology, 2013
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