Functional analyses of the NIPA1 gene with dominant negative mutations in hereditary spastic paraplegia (SPG6) and mapping within the-Prader-Willi/Angelman syndrome region.

被引：0
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作者：
Chai, JH
Rainier, S
Fink, JK
Nicholls, RD
机构：
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[2] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2225
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页码：548 / 548
页数：1
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