X-linked mental retardation (Q56270643)

https://scigraph.springernature.com/pub.10.1038/nrg1501

Europe PubMed Central

title

X-linked mental retardation (English)

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author name string

H.-Hilger Ropers

series ordinal

1

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Ben C. J. Hamel

series ordinal

2

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publication date

January 2005

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published in

Nature Reviews Genetics

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volume

6

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issue

1

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page(s)

46-57

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exact match

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cites work

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Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

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Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation

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Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

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Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene

21 January 2018

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The X-linked mental retardation protein oligophrenin-1 is required for dendritic spine morphogenesis.

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21 January 2018

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21 January 2018

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21 January 2018

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Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

21 January 2018

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Neurexin mediates the assembly of presynaptic terminals

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A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

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RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

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Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

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Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation

21 January 2018

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21 January 2018

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Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing

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21 January 2018

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A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients

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IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis

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