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                                       Details for article 5 of 23 found articles
 
 
  Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload
 
 
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:
Publisher: Science China Press, Beijing
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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