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Journal Article
International Journal of Molecular Sciences, ISSN 1422-0067, 02/2019, Volume 20, Issue 4, p. 878
Lamins are fibrillary proteins that are crucial in maintaining nuclear shape and function. Recently, B-type lamin dysfunction has been linked to tauopathies.... 
tauopathy | lamins | Alzheimer’s disease | hippocampus | lamin A | LMNA | lamin C | aging
Journal Article
Family Medicine and Primary Care Review, ISSN 1734-3402, 10/2015, Volume 17, Issue 4, pp. 327 - 329
Journal Article
Revista Portuguesa de Cardiologia, ISSN 0870-2551, 09/2017, Volume 36, Issue 9, pp. 669.e1 - 669.e4
The lamin A/C (LMNA) gene encodes lamins A and C, which have an important role in nuclear cohesion and chromatin organization. Mutations in this gene usually... 
Gene LMNA | Lamin A/C | Dyslipidemia | Hypertrophic cardiomyopathy | Diabetes | Lâmina A/C | Dislipidemia | Bloqueio auriculoventricular | LMNA gene | Atrioventricular block | Miocardiopatia hipertrófica | CARDIAC & CARDIOVASCULAR SYSTEMS | PARTIAL LIPODYSTROPHY | MUSCULAR-DYSTROPHY | DILATED CARDIOMYOPATHY | LMNA MUTATIONS
Journal Article
BMC NEUROLOGY, ISSN 1471-2377, 02/2015, Volume 15, Issue 1, pp. 13 - 13
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 10/2017, Volume 70, Issue 18, pp. 2264 - 2274
Journal Article
Cytogenetic and Genome Research, ISSN 1424-8581, 04/2018, Volume 154, Issue 1, pp. 6 - 11
Many studies have shown that molecular karyotyping is an effective diagnostic tool in individuals with developmental delay/intellectual disability. We report... 
1q22q23.1 microdeletion | Congenital heart defect | RIT1 | Intellectual disability | Noonan syndrome | LMNA | GENOTYPE | CHROMOSOME-1 | PHENOTYPE | RIT1 MUTATIONS | LMNA MUTATIONS | LONG ARM | DELETION | CELL BIOLOGY | LAMIN | MICRODUPLICATION | GENETICS & HEREDITY | Index Medicus
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 02/2004, Volume 113, Issue 3, pp. 357 - 369
Laminopathies are a group of disorders caused by mutations in the LMNA gene that encodes the nuclear lamina proteins, lamin A and lamin C; their... 
MEDICINE, RESEARCH & EXPERIMENTAL | RECRUITABLE STROKE WORK | FAMILIAL PARTIAL LIPODYSTROPHY | LACKING DESMIN | HEART-FAILURE | CARDIAC MYOCYTES | ENVELOPE | DREIFUSS MUSCULAR-DYSTROPHY | GENE-EXPRESSION | HUTCHINSON-GILFORD PROGERIA | LMNA MUTATIONS | Laminopathy | LMNA gene
Journal Article
Revista Portuguesa de Cardiologia, ISSN 0870-2551, 02/2015, Volume 34, Issue 2, pp. 139.e1 - 139.e5
Introduction The LMNA gene encodes a group of proteins that have an important structural and functional role in the cell nucleus. Mutations in this gene have... 
LMNA genemutations | Dilated cardiomiopathy | Laminopathy
Journal Article
Nucleus, ISSN 1949-1034, 12/2018, Volume 9, Issue 1, pp. 277 - 288
Journal Article
Journal Article