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Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes
BACKGROUND: In the field of movement disorders, what you see (phenotype) is seldom what you get (genotype). Whereas 1 phenotype was previously associated to 1 gene, the advent of next‐generation sequencing (NGS) has facilitated an exponential increase in disease‐causing genes and genotype–phenotype...
Autores principales: | Gannamani, Rahul, van der Veen, Sterre, van Egmond, Martje, de Koning, Tom J., Tijssen, Marina A.J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015914/ https://www.ncbi.nlm.nih.gov/pubmed/33816658 http://dx.doi.org/10.1002/mdc3.13163 |
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