SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (vol 141, pg 662, 2018)

被引：0
作者：
Rebelo, Adriana P.
Saade, Dimah
Pereira, Claudia V.
Farooq, Amjad
Huff, Tyler C.
Abreu, Lisa
Moraes, Carlos T.
Mnatsakanova, Diana
Mathews, Kathy
Yang, Hua
Schon, Eric A.
Zuchner, Stephan
Shy, Michael E.
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来源：
BRAIN | 2018年 / 141卷
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D O I：
10.1093/brain/awy032
中图分类号：
R74 [神经病学与精神病学];
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页数：1
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[1]   SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency [J].
Rebelo, Adriana P. ;
Saade, Dimah ;
Pereira, Claudia V. ;
Farooq, Amjad ;
Huff, Tyler C. ;
Abreu, Lisa ;
Moraes, Carlos T. ;
Mnatsakanova, Diana ;
Mathews, Kathy ;
Yang, Hua ;
Schon, Eric A. ;
Zuchner, Stephan ;
Shy, Michael E. .
BRAIN, 2018, 141 :662-672
1