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- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Novel insights into cardiocutaneous syndromes
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia in Epidermolysis Bullosa
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