Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA

G(M2) gangliosides are a group of lysosomal lipid storage disorders that are due to mutations in HEXA, HEXB and GM2A. In our study, 10 patients with these diseases were enrolled, and Sanger sequencing was performed for the HEXA and HEXB genes. The results revealed one known splice site mutation (c.3...

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Detalles Bibliográficos
Autores principales: Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Kamgarpour, Fatemeh, Dehghanian, Fatemeh, Fardaei, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694291/
https://www.ncbi.nlm.nih.gov/pubmed/31428437
http://dx.doi.org/10.1038/hgv.2018.3

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