Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations

被引：8
|
作者：
Melo, U. S. [1 ]
Freua, F. [2 ]
Lynch, D. S. [3 ]
Ripa, B. D. [2 ]
Tenorio, R. B. [4 ]
Saute, J. A. M. [4 ]
de Souza Leite, F. [1 ]
Kitajima, J. [5 ]
Houlden, H. [3 ]
Zatz, M. [1 ]
Kok, F. [1 ,2 ,5 ]
机构：
[1] Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Hosp Clin, Neurol Dept, Neurogenet Outpatient Serv, Sao Paulo, Brazil
[3] UCL Inst Neurol, Dept Mol Neurosci, London, England
[4] Hosp Clin Porto Alegre, Serv Genet Med & Neurol, Porto Alegre, RS, Brazil
[5] Mendelics, Sao Paulo, Brazil
来源：
CLINICAL GENETICS | 2018年 / 94卷 / 05期
关键词：
ATAXIA;
D O I：
10.1111/cge.13428
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：482 / 483
页数：2
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