Case Report: Two Families With

ataxia brain diseases citrate-synthase mitochondrial diseases spastic paraplegia

Journal

Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621

Informations de publication

Date de publication:
2022
Historique:
received: 21 09 2021
accepted: 18 01 2022
entrez: 28 2 2022
pubmed: 1 3 2022
medline: 1 3 2022
Statut: epublish

Résumé

There are recent reports of associations of variants in the

Identifiants

pubmed: 35222531
doi: 10.3389/fgene.2022.780764
pii: 780764
pmc: PMC8864118
doi:

Types de publication

Case Reports

Langues

eng

Pagination

780764

Informations de copyright

Copyright © 2022 Micule, Lace, Wright, Chrestian, Strautmanis, Diriks, Stavusis, Kidere, Kleina, Zdanovica, Laflamme, Rioux, Setty, Pajusalu, Droit, Lek, Rivest and Inashkina.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer AL declared a past collaboration with one of the authors ML/ to the handling editor.

Références

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Auteurs

Ieva Micule (I)

Latvian Biomedical Research and Study Centre, Riga, Latvia.
Children's Clinical University Hospital, Riga, Latvia.

Baiba Lace (B)

Latvian Biomedical Research and Study Centre, Riga, Latvia.
Children's Clinical University Hospital, Riga, Latvia.
Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Nathan T Wright (NT)

Department of Chemistry and Biochemistry, James Madison University, Harrisonburg, VA, United States.

Nicolas Chrestian (N)

Department of Pediatric Neurology, Pediatric Neuromuscular Disorders, Centre Mère Enfant Soleil, Laval University, Québec, QC, Canada.

Jurgis Strautmanis (J)

Children's Clinical University Hospital, Riga, Latvia.

Mikus Diriks (M)

Children's Clinical University Hospital, Riga, Latvia.

Janis Stavusis (J)

Latvian Biomedical Research and Study Centre, Riga, Latvia.

Dita Kidere (D)

Latvian Biomedical Research and Study Centre, Riga, Latvia.

Elfa Kleina (E)

Latvian Biomedical Research and Study Centre, Riga, Latvia.

Anna Zdanovica (A)

Latvian Biomedical Research and Study Centre, Riga, Latvia.

Nataly Laflamme (N)

Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Nadie Rioux (N)

Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Samarth Thonta Setty (ST)

Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Sander Pajusalu (S)

Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.
Department of Clinical Genetics, Institute of Clinical Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.
Department of Genetics, Yale University School of Medicine, New Haven, CT, United States.

Arnaud Droit (A)

Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Monkol Lek (M)

Department of Genetics, Yale University School of Medicine, New Haven, CT, United States.

Serge Rivest (S)

Centre de recherche CHU de Québec, Laval University, Québec, QC, Canada.

Inna Inashkina (I)

Latvian Biomedical Research and Study Centre, Riga, Latvia.

Classifications MeSH