Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.
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Charcot-Marie-Tooth disease: New insights from skin biopsyGenotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.Diagnosis of Charcot-Marie-Tooth disease.Inherited neuropathies: clinical overview and update.Inherited neuropathies: an update.Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses.
P2860
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Rapid progression of late onse ...... n in the extracellular domain.
@ast
Rapid progression of late onse ...... n in the extracellular domain.
@en
type
label
Rapid progression of late onse ...... n in the extracellular domain.
@ast
Rapid progression of late onse ...... n in the extracellular domain.
@en
prefLabel
Rapid progression of late onse ...... n in the extracellular domain.
@ast
Rapid progression of late onse ...... n in the extracellular domain.
@en
P2093
P2860
P50
P356
P1476
Rapid progression of late onse ...... on in the extracellular domain
@en
P2093
Davide Pareyson
Matilde Laurà
Maurizio Moggio
Micaela Milani
Stefano Jann
Vidmer Scaioli
P2860
P304
P356
10.1136/JNNP.2006.112276
P407
P577
2007-11-01T00:00:00Z