CTG triplet repeat expansion in a laryngeal carcinoma from a patient with myotonic dystrophy-Reference-Cited by-同舟云学术

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CTG triplet repeat expansion in a laryngeal carcinoma from a patient with myotonic dystrophy

Published:2000-05 Issue:5 Volume:23 Page:804-806
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Osanai Ryuichi,Kinoshita Masanobu,Hirose Kazuhiko,Homma Toshio,Kawabata Isuzu

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference24 articles.

1. Massive pituitary adenoma in a patient with dystrophia myotonica

2. Intergenerational stability of the myotonic dystrophy protomutation

3. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

4. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

5. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

Cited by 21 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. Frequency and type of cancers in myotonic dystrophy: A retrospective cross‐sectional study;Muscle & Nerve;2023-03-27

2. Cancer and Myotonic Dystrophy;Journal of Clinical Medicine;2023-03-01

3. Cancer Risk in Myotonic Dystrophy Type I: Evidence of a Role for Disease Severity;JNCI Cancer Spectrum;2018-10-01

4. Imaging of the thymus in myotonic dystrophy type 1;Neurological Sciences;2017-11-25

5. Myotonic Dystrophy Type 1;Atlas of Genetic Diagnosis and Counseling;2017

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