Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene
about
Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia.Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31.Mechanisms of postural instability in hereditary spastic paraplegia.
P2860
Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
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2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Motor system abnormalities in ...... f mutation in the spastin gene
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Motor system abnormalities in ...... f mutation in the spastin gene
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type
label
Motor system abnormalities in ...... f mutation in the spastin gene
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Motor system abnormalities in ...... f mutation in the spastin gene
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prefLabel
Motor system abnormalities in ...... f mutation in the spastin gene
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Motor system abnormalities in ...... f mutation in the spastin gene
@en
P2093
P2860
P356
P1476
Motor system abnormalities in ...... f mutation in the spastin gene
@en
P2093
Navratil P
Schickel J
Schwindt A
P2860
P304
P356
10.1136/JNNP.74.8.1109
P407
P577
2003-08-01T00:00:00Z