Compound heterozygous myotonic dystrophy type 1-Reference-Cited by-同舟云学术

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Compound heterozygous myotonic dystrophy type 1

Published:2015-05-22 Issue:8 Volume:167 Page:1952-1953
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Finsterer Josef¹,Zarrouk-Mahjoub Sinda²

Affiliation:

1. Krankenanstalt Rudolfstiftung; Vienna Austria

2. UR “Human Nutrition and Metabolic Disorders” Faculty of Medicine; Laboratory of Biochemistry; Monastir Tunisie

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1;Abbruzzese;Ann Neurol,2002

2. Two is better than one: A case of homozygous myotonic dystrophy type 1;Carroll;Am J Med Genet Part A,2013

3. Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters;Cobo;Hum Mol Genet,1993

4. Left ventricular hypertrabeculation in myotonic dystrophy type 1;Finsterer;Herz,2001

5. Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1;Groh;N Engl J Med,2008

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