Exclusion of COL7A1 mutation in Kindler syndrome - ScienceDirect
Kindlin-1 and Its Role in Kindler Syndrome | Plastic Surgery Key
Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome - ScienceDirect
Figure 1. [Characteristic clinical features of Kindler syndrome]. - GeneReviews® - NCBI Bookshelf
A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina - Valinotto - 2020 - Pediatric Dermatology - Wiley Online Library
Kindler Syndrome (Poikiloderma, hereditary acrokeratotic; Bullous acrokeratotic poikiloderma of Kindler and Weary; Poikiloderma, congenital with bullae Weary type) - Dermatology Advisor
Novel and Recurrent FERMT1 Gene Mutations in Kindler Syndrome
Kindler's syndrome: A tale of two siblings Handa N, Kachhawa D, Jain VK, Rao P, Das A - Indian J Dermatol
Clinical features of Kindler syndrome. a, b Poikiloderma with... | Download Scientific Diagram
Loss-of-Function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation - The American Journal of Pathology
Nailfold capillaroscopic changes in Kindler syndrome. - Abstract - Europe PMC
Mild Clinical Phenotype of Kindler Syndrome Associated with Late Diagnosis and Skin Cancer | Semantic Scholar