The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred-Reference-Cited by-同舟云学术

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The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred

Published:1997-08-01 Issue:2 Volume:49 Page:552-558
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

McLean C. A.,Storey E.,Gardner R.J.M.,Tannenberg A. E.G.,Cervenakova L.,Brown P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 68 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. Genetics of Prion Disease;Prions and Diseases;2023

2. Genetic counseling for prion disease: Updates and best practices;Genetics in Medicine;2022-10

3. Fatal Familial Insomnia;Autonomic Nervous System and Sleep;2021

4. Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype;Prion;2020-01-01

5. Prion diseases;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

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