(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients-Reference-Cited by-同舟云学术

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(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients

Published:1993-08 Issue:1 Volume:50 Page:85-92
ISSN:0885-4505
Container-title:Biochemical Medicine and Metabolic Biology
language:en
Short-container-title:Biochemical Medicine and Metabolic Biology

Author:

Novelli G.,Gennarelli M.,Menegazzo E.,Mostacciuolo M.L.,Pizzuti A.,Fattorini C.,Tessarolo D.,Tomelleri G.,Giacanelli M.,Danieli G.A.,Rizzuto N.,Caskey C.T.,Angelini C.,Dallapiccola B.

Publisher

Elsevier BV

Subject

Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 50 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. Myotonic Dystrophies;Current Clinical Neurology;2023

2. Genitourinary and lower gastrointestinal conditions in patients with myotonic dystrophy type 1: A systematic review of evidence and implications for clinical practice;Neuromuscular Disorders;2022-05

3. Predicting daytime sleepiness and fatigue: a 9-year prospective study in myotonic dystrophy type 1;Journal of Neurology;2019-10-31

4. The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care;Orphanet Journal of Rare Diseases;2019-06-03

5. Social cognition in myotonic dystrophy type 1: Specific or secondary impairment?;PLOS ONE;2018-09-24

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