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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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Title: |
Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload |
Author: |
Li, Hongyu Ma, Qingwen Xue, Yan Cai, Linlin Bao, Liwen Hong, Lei Zeng, Yitao Huang, Shu-Zhen Finnell, Richard H. Zeng, Fanyi |
Appeared in: |
Science China life sciences |
Paging: |
Volume 68 () nr. 2 pages 484-501 |
Year: |
2024-10-11 |
Contents: |
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Publisher: |
Science China Press, Beijing |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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