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Phenotype–genotype discrepancies in the prospective Huntington at‐risk observational study
OBJECTIVE: To examine phenotype–genotype discrepancies (PGDs) wherein genotype‐concealed and prospective judgments of the motor onset of Huntington disease (HD) occurred among at‐risk adults who had nonexpanded (<37) cytosine–adenine–guanine (CAG) trinucleotide DNA repeats. METHODS: We examined t...
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| Publicado no: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6562068/ https://ncbi.nlm.nih.gov/pubmed/31211168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.781 |
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