Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

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Curvilinear Association Between Language Disfluency and CGG Repeat Size Across the Normal, Intermediate, and Premutation Range

P2860

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P2860

Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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Screening for intermediate CGG ...... an patients with Parkinsonism.

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P1476

Screening for intermediate CGG ...... ian patients with Parkinsonism

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P2093

Hossein Darvish

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Mahmoud Shekari Khaniani

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Sima Mansoori Derakhshan

http://www.w3.org/2001/XMLSchema#string

Tayyeb Bahrami

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P2860

The fragile-X premutation: a maturing perspective.

A simple salting out procedure for extracting DNA from human nucleated cells

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

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.

Advances in understanding the molecular basis of FXTAS

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

Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism

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

Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.

P2888

s10072-016-2723-6

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123-128

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scholarly article

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10.1007/S10072-016-2723-6

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http://www.w3.org/2001/XMLSchema#string

P478

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Atefeh Entezari

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2016-10-01T00:00:00Z

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27696273

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Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

about

P2860

P2860

Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

description

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type

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698