Additional file 1 of Novel biallelic TK2 mutations cause mitochondrial DNA depletion syndrome with infantile early-onset lipid storage myopathy

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Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28613284
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00
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article

Additional file 1 of Novel biallelic TK2 mutations cause mitochondrial DNA depletion syndrome with infantile early-onset lipid storage myopathy

Figshare
Mitochondrial Function and Pathology
article

Additional file 1 of Novel biallelic TK2 mutations cause mitochondrial DNA depletion syndrome with infantile early-onset lipid storage myopathy

article en

Abstract

No abstract available for this paper.
Figshare
Qilu Hospital of Shandong University (CN)
Zero hunger
Openalex Percentile: Top 53%
Mitochondrial Function and Pathology
DOIOpen Access PDFOpenAlex
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Additional file 1 of Novel biallelic TK2 mutations cause mitochondrial DNA depletion syndrome with infantile early-onset lipid storage myopathy · Figshare (2025) | TGRS Research Map | TGRS