Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.
about
An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogsA HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth diseaseElectrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis.EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts.Nuclear envelope proteins and neuromuscular diseases.Dominantly inherited peripheral neuropathies.Mutation Analysis of Gap Junction Protein Beta 1 and Genotype-Phenotype Correlation in X-linked Charcot-Marie-Tooth Disease in Chinese PatientsThe homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature review.AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3.Charcot-Marie-Tooth disease type 4C in Japan: report of a case.Inherited polyneuropathy in Leonberger dogs.Nerve conduction abnormalities in aging mice deficient for myelin-associated glycoprotein.Loss of large-diameter spindle afferent fibres is not detrimental to the control of body sway during upright stance: evidence from neuropathy.
P2860
Q21144864-962154CB-58F3-4C94-ADCC-EC8DAD11A2B8Q33909995-107FCF2C-AE75-4104-8EA2-A85A06A94B92Q34044153-40411F62-880E-4DC7-B929-EEE1D4003C67Q34368117-44A03070-D33F-4195-82EC-3C0E17FD6D3EQ35093315-70A3161D-DAFF-4149-8B8F-CF5587F01C49Q35193592-5709F16C-8226-4519-9219-CBFFD19ABB25Q36856529-A17DDDAE-2EE0-48E8-801F-3ED27B3B5D33Q37826603-1174B8E0-F079-43FC-9731-F80A67EC12DCQ43169359-46575A37-CB3B-4401-BDC4-9DD4A6EDE9AEQ43830039-332D3AE1-330B-4FF6-979C-FB31920C65B3Q43882092-853FF9CF-668B-4F3D-A01E-FD972682D68FQ48788255-B1F3D517-8477-436C-A1F2-6864E18CBBF5Q49130475-4ADD8E06-1DBC-47CB-9C5A-E06B42E755CD
P2860
Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@ast
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@en
type
label
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@ast
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@en
prefLabel
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@ast
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@en
P2860
P1433
P1476
Charcot-marie-tooth disease an ...... for distinction and diagnosis.
@en
P2093
D Pareyson
P2860
P304
P356
10.1002/(SICI)1097-4598(199911)22:11<1498::AID-MUS4>3.0.CO;2-9
P577
1999-11-01T00:00:00Z