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Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 64-67, 2022.
Artículo en Chino | WPRIM | ID: wpr-928363
ABSTRACT
OBJECTIVE@#To explore the genetic basis for a Chinese pedigree affected with dyschromatosis symmetrica hereditaria (DSH).@*METHODS@#PCR and Sanger sequencing were carried out for the proband, and suspected variant was validated by Sanger sequencing in the pedigree.@*RESULTS@#The proband was found to harbor a novel variant of c.1352delA (p.N451Mfs*13) of the ADAR (NM_001111) gene. The same variant was found in her affected mother and sister, but not in her unaffected father, uncle, and 100 healthy individual.@*CONCLUSION@#The novel variant of the ADAR gene probably underlay the pathogenesis of DSH in this pedigree.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Trastornos de la Pigmentación / Adenosina Desaminasa / China / Proteínas de Unión al ARN / Mutación Límite: Femenino / Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2022 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Trastornos de la Pigmentación / Adenosina Desaminasa / China / Proteínas de Unión al ARN / Mutación Límite: Femenino / Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2022 Tipo del documento: Artículo