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X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
X linked hereditary spastic paraplegia is a rare condition that has been divided into two forms (the pure spastic form and the complicated form) as a function of clinical course and severity. A gene for pure hereditary spastic paraplegia (SPG2) has been mapped to the proximal long arm of the X chrom...
Gorde:
| Argitaratua izan da: | J Med Genet |
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| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMJ Publishing Group
1993
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016372/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8320699/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.5.381 |
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