Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease. - Wikidata - wikimedia - TriplyDB

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

http://www.wikidata.org/entity/Q33646656

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Nine-hole Peg Test and Ten-meter Walk Test for Evaluating Functional Loss in Chinese Charcot-Marie-Tooth Disease An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical features.

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P2860

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

http://www.wikidata.org/entity/Q33646656

description

2017 nî lūn-bûn

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2017 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2017 թվականի մայիսին հրատարակված գիտական հոդված

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2017年の論文

@ja

2017年論文

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2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

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2017年論文

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2017年论文

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name

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

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type

label

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

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prefLabel

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

@en

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Chinese Medical Journal

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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

@en

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He Lyu

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Jing Liu

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Su-Qin Jin

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Wei Zhang

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Yuan-Yuan Lu

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Yue-Huan Zuo

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Yun Yuan

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Zhao-Xia Wang

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P2860

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Hereditary Transthyretin Amyloidosis in Eight Chinese Families.

A retrospective review of X-linked Charcot-Marie-Tooth disease in childhood.

Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report

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.

Mutation Analysis of Gap Junction Protein Beta 1 and Genotype-Phenotype Correlation in X-linked Charcot-Marie-Tooth Disease in Chinese Patients

Improving molecular diagnosis of Chinese patients with Charcot-Marie-Tooth by targeted next-generation sequencing and functional analysis

Compound Heterozygote Mutation of C12orf65 Causes Distal Motor Neuropathy and Optic Atrophy

A Review of X-linked Charcot-Marie-Tooth Disease.

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1049-1054

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scholarly article

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10.4103/0366-6999.204925

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9

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130

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2017-05-01T00:00:00Z

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28469099

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5421174

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