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/vufind/Search/Results?lookfor=%22Cao%2C+Wanqian%22&type=Person&sort=year
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PubPharm (11)
1
The MORC2 p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathways
enthalten in:
Neural regeneration research
| 2024
von
Zeng, S.
|
Yang, H.
|
Wang, B.
| +8
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2
Expanding the genetic and clinical spectrum of SORD-related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement
enthalten in:
Journal of the peripheral nervous system : JPNS
| 2023
von
Li, L.
|
Xie, Y.
|
Zeng, S.
| +9
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3
Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease
enthalten in:
Journal of the peripheral nervous system : JPNS
| 2023
von
Tian, Y.
|
Hou, X.
|
Cao, W.
| +43
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4
Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review
enthalten in:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
| 2023
von
Cao, W.
|
Huang, S.
|
Zhao, H.
| +4
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5
Expanding the genetic and clinical spectrum of SORD‐related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement
enthalten in:
Journal of the Peripheral Nervous System
| 2023
von
Li, L.
|
Xie, Y.
|
Zeng, S.
| +9
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6
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease
enthalten in:
Journal of the Peripheral Nervous System
| 2023
von
Tian, Y.
|
Hou, X.
|
Cao, W.
| +43
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7
Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China
enthalten in:
European journal of neurology
| 2021
von
Xie, Y.
|
Lin, Z.
|
Liu, L.
| +19
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8
One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families
enthalten in:
Frontiers in neurology
| 2021
von
Xie, Y.
|
Lin, Z.
|
Li, X.
| +10
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9
Genotype and phenotype distribution of 435 patients with Charcot–Marie–Tooth disease from central south China
enthalten in:
European Journal of Neurology
| 2021
von
Xie, Y.
|
Lin, Z.
|
Liu, L.
| +19
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10
Research advance of underlying pathogenesis and target therapies in Charcot-Marie-Tooth disease type 1A
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2020
von
Cao, W.
|
Zhang, R.
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Zeitschriftentitel
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Frontiers in neurology
2
Journal of the Peripheral Nervous System
2
Journal of the peripheral nervous system : JPNS
1
European Journal of Neurology
1
European journal of neurology
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distal hereditary motor neuropathy
1
506T60A25R
1
Adaptor Proteins, Signal Transducing
1
Apoptosis Regulatory Proteins
1
BAG3 protein, human
1
Charcot-Marie-Tooth disease
1
Charcot-Marie-Tooth disease 2Z
1
Charcot-Marie-Tooth disease type 2
1
Charcot-Marie-Tooth diseases
1
Charcot-Marie-tooth disease
1
DNA-Binding Proteins
1
EC 1.1.1.14
1
GARS
1
IGHMBP2 protein, human
1
L-Iditol 2-Dehydrogenase
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2024
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2020
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