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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Detaylı Bibliyografya
Yayımlandı:Ann Clin Transl Neurol
Asıl Yazarlar: Shoulson, Ira, Eberly, Shirley, Oakes, David, Kayson, Elise, Young, Anne B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2019
Konular:
Research Articles
Online Erişim: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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