A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis.

Morice-Picard, Fanny; Lanvin, Pierre-Louis; Lasseaux, Eulalie; Boralevi, Franck; Léauté-Labrèze, Christine; Lebreton, Louis

Morice-Picard, Fanny; Lanvin, Pierre-Louis; Lasseaux, Eulalie; Boralevi, Franck; Léauté-Labrèze, Christine; Lebreton, Louis.

Afiliación

Morice-Picard F; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Lanvin PL; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Lasseaux E; Departments of Medical Genetics, Hôpital Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Boralevi F; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Léauté-Labrèze C; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Lebreton L; Departments of Biochemistry, Hôpital Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.

Clin Exp Dermatol ; 48(9): 1087-1089, 2023 08 25.

Article en En | MEDLINE | ID: mdl-37140446

Asunto(s)

Hipotricosis; Humanos; Hipotricosis/genética; Cabello; Mutación; Linaje

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hipotricosis Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Exp Dermatol Año: 2023 Tipo del documento: Article País de afiliación: Francia

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