Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.
about
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation conditionXLMR genes: update 2007.MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome.SNPs in human miRNA genes affect biogenesis and functionMicroRNAs: a light into the "black box" of neuropediatric diseases?Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?Genetic variations of microRNAs in human cancer and their effects on the expression of miRNAs.Genetic variants in miR-146a, miR-149, miR-196a2, miR-499 and their influence on relative expression in lung cancers.
P2860
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P2860
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.
description
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name
Mutation screening of brain-ex ...... c X-linked mental retardation.
@en
Mutation screening of brain-ex ...... c X-linked mental retardation.
@nl
type
label
Mutation screening of brain-ex ...... c X-linked mental retardation.
@en
Mutation screening of brain-ex ...... c X-linked mental retardation.
@nl
prefLabel
Mutation screening of brain-ex ...... c X-linked mental retardation.
@en
Mutation screening of brain-ex ...... c X-linked mental retardation.
@nl
P2093
P2860
P356
P1476
Mutation screening of brain-ex ...... c X-linked mental retardation.
@en
P2093
Andreas W Kuss
Arjan de Brouwer
Bettina Moser
Claude Moraine
H Hilger Ropers
Jamel Chelly
Jean-Pierre Fryns
Lars R Jensen
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201758
P577
2006-12-20T00:00:00Z