Molecular genetic analysis of Charcot–Marie–Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging-Reference-Cited by-同舟云学术

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Molecular genetic analysis of Charcot–Marie–Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging

Published:2001-07 Issue:1-2 Volume:188 Page:21-26
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Aarskog N.K,Aadland S,Gjerde I.O,Vedeler C.A

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference50 articles.

1. Genetic and clinical aspects of Charcot–Marie–Tooth's disease;Skre;Clin. Genet.,1974

2. Peripheral neuropathy;Dyck,1992

3. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding;Brain,1980

4. Hereditary motor and sensory neuropathies. Present status of types I, II and III;Gabreels-Festen;Clin. Neurol. Neurosurg.,1993

5. DNA duplication associated with Charcot–Marie–Tooth disease type 1A;Lupski;Cell,1991

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pregnancies and deliveries in patients with Charcot-Marie-Tooth disease;Neurology;2005-02-07

2. Hereditary Motor and Sensory Neuropathies Involving Altered Dosage or Mutation of PMP22: The CMT1A Duplication and HNPP Deletion;Peripheral Neuropathy;2005

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