Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability-Reference-Cited by-同舟云学术

Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability

Published:2019-04 Issue: Volume:399 Page:69-75
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Tolomeo D.,Rubegni A.,Severino M.,Pochiero F.,Bruno C.,Cassandrini D.,Madeo A.,Doccini S.,Pedemonte M.,Rossi A.,D'Amore F.,Donati M.A.,Di Rocco M.,Santorelli F.M.^ORCID,Nesti C.^ORCID

Funder

Italian Ministry of Health

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference29 articles.

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5. Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy;Fassone;J. Med. Genet.,2011

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2. Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation;Neurological Sciences;2022-07-31

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