MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes.
about
Epigenetic mechanisms in diurnal cycles of metabolism and neurodevelopmentPhenotypic and molecular convergence of 2q23.1 deletion syndrome with other neurodevelopmental syndromes associated with autism spectrum disorder.Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.Clinical and Molecular Aspects of MBD5-Associated Neurodevelopmental Disorder (MAND).The Mendelian disorders of the epigenetic machinery.RAI1 Overexpression Promotes Altered Circadian Gene Expression and Dyssomnia in Potocki-Lupski Syndrome.
P2860
MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
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2014年论文
@zh-cn
name
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@ast
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@en
type
label
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@ast
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@en
prefLabel
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@ast
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@en
P2093
P2860
P356
P1476
MBD5 haploinsufficiency is ass ...... genis and fragile X syndromes.
@en
P2093
Brooke Burns
David L Nelson
Loren Pugliesi
Raiha Tahir
Sureni V Mullegama
Yanghong Gu
Zalak Shah
P2860
P2888
P304
P356
10.1038/EJHG.2014.200
P577
2014-10-01T00:00:00Z
P5875
P6179
1045643243