Identification and characterization of novel alternative splice variants of human SAMD11.
about
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis PigmentosaGene expression changes during retinal development and rod specification.
P2860
Identification and characterization of novel alternative splice variants of human SAMD11.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
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2013年论文
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2013年论文
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name
Identification and characterization of novel alternative splice variants of human SAMD11.
@en
Identification and characterization of novel alternative splice variants of human SAMD11.
@nl
type
label
Identification and characterization of novel alternative splice variants of human SAMD11.
@en
Identification and characterization of novel alternative splice variants of human SAMD11.
@nl
prefLabel
Identification and characterization of novel alternative splice variants of human SAMD11.
@en
Identification and characterization of novel alternative splice variants of human SAMD11.
@nl
P2093
P1433
P1476
Identification and characterization of novel alternative splice variants of human SAMD11.
@en
P2093
Chongde Long
Guorong Jin
Huangxuan Shen
Qingjiong Zhang
Weiwei Liu
Yujuan Zhu
P304
P356
10.1016/J.GENE.2013.08.033
P407
P577
2013-08-23T00:00:00Z