Familial comedonal Darier's disease: a new ATP2A2 mutation with intra-family clinical heterogeneity

Int J Dermatol. 2023 Dec;62(12):e620-e621. doi: 10.1111/ijd.16712. Epub 2023 May 3.

Authors

Maria B Civico-Ruiz¹, Teresa Zulueta-Dorado², Juan J López-Delgado², Francisco Fernández-Rosado³, Isabel M Coronel-Pérez¹, María L Martínez-Barranca¹

Affiliations

¹ Department of Dermatology, Ntra Sra de Valme Hospital, Seville, Spain.
² Department of Pathology, Virgen de Rocio Hospital, Seville, Spain.
³ Lorgen G.P, Granada, Spain.

PMID: 37132526
DOI: 10.1111/ijd.16712

No abstract available

Publication types

Letter

MeSH terms

Darier Disease* / diagnosis
Darier Disease* / genetics
Humans
Mutation
Sarcoplasmic Reticulum Calcium-Transporting ATPases / genetics

Substances

Sarcoplasmic Reticulum Calcium-Transporting ATPases
ATP2A2 protein, human