Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome

Detalles Bibliográficos
Autores principales: Dohrn, Maike F., Beijer, Danique, Mulahasanovic, Lejla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Comment
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272550/
https://www.ncbi.nlm.nih.gov/pubmed/35811324
http://dx.doi.org/10.1186/s42466-022-00197-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272550/
https://www.ncbi.nlm.nih.gov/pubmed/35811324
http://dx.doi.org/10.1186/s42466-022-00197-6

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