A genetic study of torsion dystonia.
A family study of 32 patients with torsion dystonia has shown at least two forms of generalized dystonia with onset in childhood. These two forms, an autosomal dominant and an autosomal recessive, are clinically indistinguishable. There were at least three families and probably about six to eight pa...
שמור ב:
| הוצא לאור ב: | J Med Genet |
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| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
1975
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013226/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1121020/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.12.1.12 |
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