Double Trouble in Hereditary Neuropathy-Reference-Cited by-同舟云学术

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Double Trouble in Hereditary Neuropathy

Published:2006-01-01 Issue:1 Volume:63 Page:112
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Hodapp Julie A.,Carter Gregory T.,Lipe Hillary P.,Michelson Sara J.,Kraft George H.,Bird Thomas D.

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 57 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. Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian Cohort;Neurology India;2023

2. One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families;Frontiers in Neurology;2022-01-28

3. Coexistence of Charcot-Marie-Tooth 1A and nondystrophic myotonia due to PMP22 duplication and SCN4A pathogenic variants: a case report;BMC Neurology;2022-01-07

4. Novel insights into the genetic profile of hereditary spastic paraplegia in India;Journal of Neurogenetics;2022-01-02

5. Genetic spectrum of inherited neuropathies in India;Annals of Indian Academy of Neurology;2022

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