A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

about

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

Item

http://www.wikidata.org/entity/Q40715457

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

@en

type

Item

label

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

@en

prefLabel

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

@en

P1476

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

@en

P2093

F Marrosu

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

G C Coghe

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

G Fenu

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

J Frau

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

L Lorefice

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

M G Marrosu

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

M R Murru

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

M Rolesu

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

S Tranquilli

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

P2860

Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)

Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”

Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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

Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates.

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

FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.

P2888

s10072-015-2339-2

P304

2213-2220

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

P31

scholarly article

P356

10.1007/S10072-015-2339-2

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

P433

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

P478

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

P50

Eleonora Cocco

P577

2015-07-21T00:00:00Z

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

P698

26194536

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