Comparison of CTG Repeat Length Expansion and Clinical Progression of Myotonic Dystrophy Over a Five Year Period.

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.32.8.593
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Facial Emotion Recognition in Myotonic Dystrophy Type 1 Correlates With CTG Repeat Expansion

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2006English

Instability of the (CTG)n Repeat in Congenital Myotonic Dystrophy

American Journal of Human Genetics
Genetics
1997English

Replacement of the Myotonic Dystrophy Type 1 CTG Repeat With 'Non-CTG Repeat' Insertions in Specific Tissues

Journal of Medical Genetics
Genetics
2011English

Clinical Progression of Giant-Axonal Neuropathy Over a Twelve Year Period

Canadian Journal of Neurological Sciences
MedicineNeurology
1981English

Analysis of CTG Repeat Length Variation in the DMPK Gene in the General Population and the Molecular Diagnosis of Myotonic Dystrophy Type 1 in Malaysia

BMJ Open
Medicine
2017English

Minimal Expression of Myotonic Dystrophy: A Clinical and Molecular Analysis.

Journal of Medical Genetics
Genetics
1992English

Expansion of the Myotonic Dystrophy Gene in Italian and Spanish Patients.

Journal of Medical Genetics
Genetics
1992English

Carcinoma of the Lung: A Review of the Five-Year Survivals Over a 15-Year Period

Diseases of the Chest
1967English

Development of Pharmacophore Models for Small Molecules Targeting RNA: Application to the RNA Repeat Expansion in Myotonic Dystrophy Type 1

Bioorganic and Medicinal Chemistry Letters
Organic ChemistryMolecular MedicineMolecular BiologyBiochemistryClinical BiochemistryPharmaceutical ScienceDrug Discovery
2016English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy