Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Detalles Bibliográficos
Autores principales: Huang, Lijia, Warman-Chardon, Jodi, Carter, Melissa T., Friend, Kathie L., Dudding, Tracy E., Schwartzentruber, Jeremy, Zou, Ruobing, Schofield, Peter W., Douglas, Stuart, Bulman, Dennis E., Boycott, Kym M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966260/
https://www.ncbi.nlm.nih.gov/pubmed/35351177
http://dx.doi.org/10.1186/s13023-022-02297-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966260/
https://www.ncbi.nlm.nih.gov/pubmed/35351177
http://dx.doi.org/10.1186/s13023-022-02297-7

Ejemplares similares