Found: 8
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LMNA-related dilated cardiomyopathy.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066499
- By:
- Publication type:
- Article
Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 15, p. 3334, doi. 10.3390/jcm10153334
- By:
- Publication type:
- Article
New Deletion in LAMP2 Causing Familial Danon Disease. Effect of X-Chromosome Inactivation.
- Published in:
- Folia Medica, 2022, v. 64, n. 5, p. 853, doi. 10.3897/folmed.64.e66292
- By:
- Publication type:
- Article
Splicing mutation in TAZ gene leading to exon skipping and Barth syndrome.
- Published in:
- Acta Myologica, 2021, v. 40, n. 2, p. 88, doi. 10.36185/2532-1900-047
- By:
- Publication type:
- Article
Novel desmoplakin mutations in familial Carvajal syndrome.
- Published in:
- Acta Myologica, 2018, v. 37, n. 4, p. 263
- By:
- Publication type:
- Article
Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene.
- Published in:
- Acta Myologica, 2017, v. 36, n. 4, p. 207
- By:
- Publication type:
- Article
Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland.
- Published in:
- Biomedicines, 2024, v. 12, n. 6, p. 1355, doi. 10.3390/biomedicines12061355
- By:
- Publication type:
- Article