标题
The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
作者
关键词
Autism Spectrum Disorder, Mild Intellectual Disability, Neuritic Process, Exome Aggregation Consortium, GATK HaplotypeCaller
出版物
Molecular Neurodegeneration
Volume 10, Issue 1, Pages -
出版商
Springer Nature
发表日期
2015-09-24
DOI
10.1186/s13024-015-0045-4
参考文献
相关参考文献
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