Associated Papers
Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutations.
Colombo EA et al.
Orphanet Journal of Rare Diseases, 2016
Recently Identified Forms of Epidermolysis Bullosa.
McGrath JA
Annals of Dermatology, 2015
Crucial role of posttranslational modifications of integrin α3 in interstitial lung disease and nephrotic syndrome.
Yalcin EG et al.
Human Molecular Genetics, 2015
Integrin α3 mutations with kidney, lung, and skin disease.
Has C et al.
The New England Journal of Medicine, 2012
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