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Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes

BACKGROUND: Progress in genetics – particularly the advent of next‐generation sequencing (NGS) – has enabled an unparalleled gene discovery and revealed unmatched complexity of genotype–phenotype correlations in movement disorders. Among other things, it has emerged that mutations in one and the sam...

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Detalhes bibliográficos
Publicado no:Mov Disord Clin Pract
Main Authors: Magrinelli, Francesca, Balint, Bettina, Bhatia, Kailash P.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8015894/
https://ncbi.nlm.nih.gov/pubmed/33816657
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.13165
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