Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
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Overview of Charcot-Marie-Tooth disease type 1A.Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study.Inherited neuropathies: the interface between molecular genetics and pathology.Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.Electromyographic tendon reflex recording: An accurate and comfortable method for diagnosis of charcot-marie-tooth disease type 1a.
P2860
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
description
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name
Duplication of part of chromos ...... t-Marie-Tooth disease type 1).
@en
Duplication of part of chromos ...... and sensory neuropathy type I
@nl
type
label
Duplication of part of chromos ...... t-Marie-Tooth disease type 1).
@en
Duplication of part of chromos ...... and sensory neuropathy type I
@nl
prefLabel
Duplication of part of chromos ...... t-Marie-Tooth disease type 1).
@en
Duplication of part of chromos ...... and sensory neuropathy type I
@nl
P2093
P356
P1433
P1476
Duplication of part of chromos ...... t-Marie-Tooth disease type 1).
@en
P2093
P304
P356
10.1002/ANA.410310518
P577
1992-05-01T00:00:00Z