Emerging Role of ODC1 in Neurodevelopmental Disorders and Brain Development

Ornithine decarboxylase 1 (ODC1 gene) has been linked through gain-of-function variants to a rare disease featuring developmental delay, alopecia, macrocephaly, and structural brain anomalies. ODC1 has been linked to additional diseases like cancer, with growing evidence for neurological contributio...

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Detalles Bibliográficos
Autores principales: Prokop, Jeremy W., Bupp, Caleb P., Frisch, Austin, Bilinovich, Stephanie M., Campbell, Daniel B., Vogt, Daniel, Schultz, Chad R., Uhl, Katie L., VanSickle, Elizabeth, Rajasekaran, Surender, Bachmann, André S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064465/
https://www.ncbi.nlm.nih.gov/pubmed/33806076
http://dx.doi.org/10.3390/genes12040470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064465/
https://www.ncbi.nlm.nih.gov/pubmed/33806076
http://dx.doi.org/10.3390/genes12040470

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