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DRD2 NM_000795.3:c.957C>T

Known as: NM_000795.3:c.957C>T, DRD2 957T Indel Mutation, DRD2 C957T Indel Mutation 
A nucleotide substitution at position 957 of the coding sequence of the DRD2 gene where cytosine has been mutated to thymine.
National Institutes of Health

Papers overview

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2017
2017
Please cite this article as: Johanna Inhyang Kim, Jae-Won Kim, Jong-Min Lee, Hyuk Jin Yun, Chul-ho Sohn, Min-Sup Shin, Bongseog… 
2015
2015
插入/缺失(insertion/deletion,InDel)多态性是指基因组中插入或缺失不同大小的 DNA 片段所形成的多态性遗传标记[1]。InDel 为一种特殊类型的二等位基因遗传标记,PCR… 
Review
2013
Review
2013
This peer-reviewed article can be downloaded, printed and distributed freely for any purposes (see copyright notice below… 
2005
2005
Edicion financiada por el Ministerio de Educacion y Ciencia con cargo al "Plan Nacional de I+D+I 2004-2007".