In Silico Examination of Single Nucleotide Missense Mutations in NHLH2, a Gene Linked to Infertility and Obesity

Continual advances in our understanding of the human genome have led to exponential increases in known single nucleotide variants. The characterization of each of the variants lags behind. For researchers needing to study a single gene, or multiple genes in a pathway, there must be ways to narrow do...

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Detalles Bibliográficos
Autores principales: Madsen, Allison T., Good, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968165/
https://www.ncbi.nlm.nih.gov/pubmed/36834605
http://dx.doi.org/10.3390/ijms24043193

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968165/
https://www.ncbi.nlm.nih.gov/pubmed/36834605
http://dx.doi.org/10.3390/ijms24043193

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