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Hereditary inclusion body myopathy in Persian Jews: a case report from Iran
被引:0
|
作者
:
论文数:
引用数:
h-index:
机构:
Miryounesi, M.
[
1
]
Soltanzadeh, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Maryland, Dept Neurol, Baltimore, MD 21201 USA
Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
Soltanzadeh, P.
[
2
]
Modarressi, M. H.
论文数:
0
引用数:
0
h-index:
0
机构:
Tehran Univ Med Sci Tehran, Sch Med, Dept Med Genet, Tehran, Iran
Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
Modarressi, M. H.
[
3
]
机构
:
[1]
Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[2]
Univ Maryland, Dept Neurol, Baltimore, MD 21201 USA
[3]
Tehran Univ Med Sci Tehran, Sch Med, Dept Med Genet, Tehran, Iran
来源
:
CLINICAL GENETICS
|
2014年
/ 85卷
/ 06期
关键词
:
D O I
:
10.1111/cge.12220
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:595 / 597
页数:3
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