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Publications by Sophia Aristodemou

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American Journal of Human Genetics
Genetics
2014English

Safety and Early Efficacy Outcomes for Lentiviral Fibroblast Gene Therapy in Recessive Dystrophic Epidermolysis Bullosa

JCI insight
Medicine
2019English

Recessive Mutation in Tetraspanin CD151 Causes Kindler Syndrome-Like Epidermolysis Bullosa With Multi-Systemic Manifestations Including Nephropathy

Matrix Biology
Molecular Biology
2018English

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2017English

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