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Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload |
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Titel: |
Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload |
Auteur: |
Li, Hongyu Ma, Qingwen Xue, Yan Cai, Linlin Bao, Liwen Hong, Lei Zeng, Yitao Huang, Shu-Zhen Finnell, Richard H. Zeng, Fanyi |
Verschenen in: |
Science China life sciences |
Paginering: |
Jaargang 68 () nr. 2 pagina's 484-501 |
Jaar: |
2024-10-11 |
Inhoud: |
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Uitgever: |
Science China Press, Beijing |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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