RAD51 haploinsufficiency causes congenital mirror movements in humans.
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Diseases associated with defective responses to DNA damageA Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous RecombinationA novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's diseaseA never-ending story: the steadily growing family of the FA and FA-like genesInterhemispheric control of unilateral movement.Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the LiteratureSelective chromatid segregation mechanism invoked for the human congenital mirror hand movement disorder development by RAD51 mutations: a hypothesisThe promise of whole-exome sequencing in medical genetics.A novel role for the DNA repair gene Rad51 in Netrin-1 signalling.Exome sequencing greatly expedites the progressive research of Mendelian diseases.One hand clapping: lateralization of motor control.Personalised Medicine: Genome Maintenance Lessons Learned from Studies in Yeast as a Model Organism.The corticospinal tract: Evolution, development, and human disorders.Haploinsufficiency of Tumor Suppressor Genes is Driven by the Cumulative Effect of microRNAs, microRNA Binding Site Polymorphisms and microRNA Polymorphisms: An In silico Approach.Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder.Congenital mirror movements: lack of decussation of pyramids.RAD51 deficiency disrupts the corticospinal lateralization of motor control.DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.Mutations in the netrin-1 gene cause congenital mirror movements.Structural Neural Correlates of Physiological Mirror Activity During Isometric Contractions of Non-Dominant Hand Muscles.Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation
P2860
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P2860
RAD51 haploinsufficiency causes congenital mirror movements in humans.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
RAD51 haploinsufficiency causes congenital mirror movements in humans.
@en
type
label
RAD51 haploinsufficiency causes congenital mirror movements in humans.
@en
prefLabel
RAD51 haploinsufficiency causes congenital mirror movements in humans.
@en
P2093
P2860
P50
P1476
RAD51 haploinsufficiency causes congenital mirror movements in humans.
@en
P2093
Alexis Brice
Christel Depienne
Constance Flamand-Roze
Delphine Bouteiller
Emmanuel Roze
Fanny Charbonnier-Beaupel
Jean-Paul Saraiva
Marion Gaussen
Massimo Cincotta
Norbert Brueggemann
P2860
P304
P356
10.1016/J.AJHG.2011.12.002
P407
P50
P577
2012-02-02T00:00:00Z