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UnknownDe novo heterozygous pathogenic FBN1 variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case report.
Not available
S-EPMC10291322 | biostudies-literature
UnknownFactor XIII Val34Leu polymorphism and recurrent myocardial infarction in patients with coronary artery disease.
Not available
S-EPMC4295494 | biostudies-literature
UnknownCalcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis.
Not available
S-EPMC5498355 | biostudies-literature
UnknownArrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current.
Not available
S-EPMC4958519 | biostudies-literature
UnknownDisruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome.
Not available
S-EPMC11670311 | biostudies-literature
UnknownFibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis.
Not available
S-EPMC6473180 | biostudies-literature
UnknownLimited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis.
Not available
S-EPMC8156154 | biostudies-literature
UnknownTransperitoneal Versus Retroperitoneal Robotic-assisted Laparoscopic Pyeloplasty for Ureteropelvic Junction Obstruction in Children. A Multicentre, Prospective Study.
Not available
S-EPMC9257661 | biostudies-literature
UnknownAntisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Not available
S-EPMC6614138 | biostudies-literature
UnknownComparative genomics of the bacterial genus Listeria: Genome evolution is characterized by limited gene acquisition and limited gene loss.
Not available
S-EPMC3019230 | biostudies-literature
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