Found: 9
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Variant Transthyretin Amyloidosis (ATTRv) in Hungary: First Data on Epidemiology and Clinical Features.
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- Genes, 2021, v. 12, n. 8, p. 1152, doi. 10.3390/genes12081152
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- Article
Differential expression of the brassinosteroid receptor-encoding BRI1 gene in Arabidopsis.
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- Planta: An International Journal of Plant Biology, 2014, v. 239, n. 5, p. 989, doi. 10.1007/s00425-014-2031-4
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- Article
Novel HCN4 gene 'splice-site' mutation causing familial bradycardia.
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- Cardiologia Croatica, 2014, v. 9, n. 5/6, p. 243, doi. 10.15836/ccar.2014.243
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- Article
Genetic screening for mutations in known long QT syndrome causing genes in patiens with known or suspected long QT syndrome with high throughput sequencing.
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- Cardiologia Croatica, 2014, v. 9, n. 5/6, p. 206, doi. 10.15836/ccar.2014.206
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- Article
The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes.
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- Diagnostics (2075-4418), 2022, v. 12, n. 5, p. N.PAG, doi. 10.3390/diagnostics12051132
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- Article
Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.
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- Canadian Journal of Physiology & Pharmacology, 2015, v. 93, n. 7, p. 569, doi. 10.1139/cjpp-2014-0527
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- Article
Direct Anticoagulants and Risk of Myocardial Infarction, a Multiple Treatment Network Meta-Analysis.
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- Angiology, 2020, v. 71, n. 1, p. 27, doi. 10.1177/0003319719874255
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- Article
Timothy syndrome 1 genotype without syndactyly and major extracardiac manifestations.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 3, p. 784, doi. 10.1002/ajmg.a.38084
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- Article
Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen–Tawil syndrome patient.
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- Cardiovascular Research, 2021, v. 117, n. 8, p. 1923, doi. 10.1093/cvr/cvaa249
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- Article