Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
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DOI：
10.1016/j.jns.2017.02.058
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发表时间：
2017-04
影响因子：
4.4
通讯作者：
T. Yamashita;J. Mitsui;N. Shimozawa;S. Takashima;H. Umemura;Kota Sato;M. Takemoto;N. Hishikawa;Y. Ohta;T. Matsukawa;H. Ishiura;J. Yoshimura;K. Doi;S. Morishita;S. Tsuji;K. Abe
中科院分区：
文献类型：
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作者：
T. Yamashita;J. Mitsui;N. Shimozawa;S. Takashima;H. Umemura;Kota Sato;M. Takemoto;N. Hishikawa;Y. Ohta;T. Matsukawa;H. Ishiura;J. Yoshimura;K. Doi;S. Morishita;S. Tsuji;K. Abe
