Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study.

about

Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study.

Item

http://www.wikidata.org/entity/Q40082437

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Molecular Epidemiology of Char ...... and: A Population-Based Study.

@en

type

Item

label

Molecular Epidemiology of Char ...... and: A Population-Based Study.

@en

prefLabel

Molecular Epidemiology of Char ...... and: A Population-Based Study.

@en

P1476

Molecular Epidemiology of Char ...... and: A Population-Based Study.

@en

P2093

Kari Majamaa

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

Maria Marttila

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

Marjo Laitinen

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

Mikko Hiltunen

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

Mikko Kärppä

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

Seppo Helisalmi

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

P2860

Epidemiologic Study of Charcot-Marie-Tooth Disease: A Systematic Review

Diagnosis, natural history, and management of Charcot–Marie–Tooth disease

The validity of the Finnish Hospital Discharge Register and Causes of Death Register data on coronary heart disease.

Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.

Practice parameter: the evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, the American Association of Neuromuscular and Electrodiagnosti

Charcot-Marie-Tooth disease subtypes and genetic testing strategies

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease.

Inherited peripheral neuropathies.

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.

P304

34-39

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

P31

scholarly article

P356

10.1159/000478860

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

P433

1-2

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

P478

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

P50

Mika Kallio

Laura Kytövuori

P577

2017-08-16T00:00:00Z

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

P698

28810241

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

P921

Finland