Proteolipid protein 1 gene sequencing of hereditary spastic paraplegia☆

PCR amplification and sequencing of whole blood DNA from an individual with hereditary spastic paraplegia, as well as family members, revealed a fragment of proteolipid protein 1 (PLP1) gene exon 1, which excluded the possibility of isomer 1 expression for this family. The fragment sequence of exon...

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Detalles Bibliográficos
Autores principales: Gao, Yu, Chi, Lumei, Jin, Yinshi, Nan, Guangxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Research and Report: Neurodegenerative Diseases and Neuroregeneration
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354135/
https://www.ncbi.nlm.nih.gov/pubmed/25767481
http://dx.doi.org/10.3969/j.issn.1673-5374.2012.02.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354135/
https://www.ncbi.nlm.nih.gov/pubmed/25767481
http://dx.doi.org/10.3969/j.issn.1673-5374.2012.02.002

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