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

OBJECTIVE: The lack of epidemiological data and molecular diagnostic services in Malaysia has hampered the setting-up of a comprehensive management plan for patients with myotonic dystrophy type 1 (DM1), leading to delayed diagnosis, treatment and support for patients and families. The aim of this s...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:BMJ Open
Hoofdauteurs: Ambrose, Kathlin K, Ishak, Taufik, Lian, Lay-Hoong, Goh, Khean-Jin, Wong, Kum-Thong, Ahmad-Annuar, Azlina, Thong, Meow-Keong
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Publishing Group 2017
Onderwerpen:
Neurology
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5387946/
https://ncbi.nlm.nih.gov/pubmed/28363916
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2015-010711
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items