A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child.
about
Structural basis for substrate binding and catalytic mechanism of a human RNA:m5C methyltransferase NSun6Posttranscriptional methylation of transfer and ribosomal RNA in stress response pathways, cell differentiation, and cancerA novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract.The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.The epitranscriptome in modulating spatiotemporal RNA translation in neuronal post-synaptic function.Mutations in RNA methylating enzymes in disease.Regulation of mRNA Translation in Neurons-A Matter of Life and Death.Epitranscriptomics: A New Regulatory Mechanism of Brain Development and Function.
P2860
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P2860
A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A Novel Single-Nucleotide Dele ...... isability in an Emirati Child.
@en
type
label
A Novel Single-Nucleotide Dele ...... isability in an Emirati Child.
@en
prefLabel
A Novel Single-Nucleotide Dele ...... isability in an Emirati Child.
@en
P2093
P2860
P1476
A Novel Single-Nucleotide Dele ...... isability in an Emirati Child.
@en
P2093
Aisha M Al-Shamsi
Makanko Komara
Salma Ben-Salem
P2860
P2888
P304
P356
10.1007/S12031-015-0592-8
P577
2015-06-09T00:00:00Z
P5875
P6179
1010948332