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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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| Materias: | |
| 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 |