Recurrent central nervous system white matter changes in charcot-Marie-tooth type X disease.
about
The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and managementA Review of X-linked Charcot-Marie-Tooth Disease.Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses.Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1.MYRF is associated with encephalopathy with reversible myelin vacuolization.CNS involvement in CMTX1 caused by a novel connexin 32 mutation: a 6-year follow-up in neuroimaging and nerve conduction.
P2860
Recurrent central nervous system white matter changes in charcot-Marie-tooth type X disease.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@en
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@nl
type
label
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@en
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@nl
prefLabel
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@en
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@nl
P2093
P2860
P356
P1433
P1476
Recurrent central nervous syst ...... ot-Marie-tooth type X disease.
@en
P2093
Emily C De Los Reyes
Jennifer L McKinney
Warren D Lo
P2860
P304
P356
10.1002/MUS.24108
P577
2014-01-27T00:00:00Z