New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease (Q44261646)

1 December 2017

title

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease (English)

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1 December 2017

6

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1 December 2017

D Z Loesch

1

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1 December 2017

F Tassone

2

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J Lo

3

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H R Slater

4

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L V Hills

5

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P A Silburn

7

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G D Mellick

8

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1 December 2017

language of work or name

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25 December 2012

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1 December 2017

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volume

84

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1 December 2017

issue

4

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1 December 2017

page(s)

382-385

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Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

1 December 2017

cites work

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21 January 2018

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Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

21 January 2018

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Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

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Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond

21 January 2018

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Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers

21 January 2018

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Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

21 January 2018

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Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

21 January 2018

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Fragile X–associated tremor ataxia syndrome in FMR1 gray zone allele carriers

21 January 2018

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Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

21 January 2018

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Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?

21 January 2018

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A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

21 January 2018

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An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1).

21 January 2018

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FMR1 alleles in Parkinson's disease: relation to cognitive decline and hallucinations, a longitudinal study

21 January 2018

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FMR1 gray‐zone alleles: Association with Parkinson's disease in women?

21 January 2018

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Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China

21 January 2018

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Parkinsonism, FXTAS, and FMR1 premutations

21 January 2018

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Screen for excess FMR1 premutation alleles among males with parkinsonism

21 January 2018

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Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/CGE.12070

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1 December 2017

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