Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome
Crossref DOI link: https://doi.org/10.1186/s42466-022-00197-6
Published Online: 2022-07-11
Published Print: 2022-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Dohrn, Maike F.
Beijer, Danique
Mulahasanovic, Lejla
Text and Data Mining valid from 2022-07-11
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Article History
First Online: 11 July 2022
Declarations
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: The authors declare that they have no competing interests.