Exploration of calcium and amino acids for children with primary cardiomyopathies based on genetic characteristics. [PDF]
Jiang S +7 more
europepmc +1 more source
Novel mutation in KCNJ2 gene causes long QT interval syndrome type 7 and learning disability: A case report. [PDF]
Zhang HY, Zhang Y.
europepmc +1 more source
Unilateral Upper Extremity Paralysis Secondary to Hypokalemia and Fasting: A Case Report. [PDF]
Adler A, Shelbaya S, McCormick S.
europepmc +1 more source
Exploring the size limits of Bionano optical genome mapping to resolve alternative structures of linked interspersed chromosomal duplications. [PDF]
Pei Y +13 more
europepmc +1 more source
My Experiments in Bioelectricity: The Winding Road to Developmental Bioelectricity. [PDF]
Adams DS.
europepmc +1 more source
Functional analysis of human induced pluripotent stem cell-derived cardiac tissue during endothelial cell network changes. [PDF]
Koike T +6 more
europepmc +1 more source
Genetic Association Study Between Refractive Error-Related Genes and High Myopia in the Chinese Han Population. [PDF]
Liu J +11 more
europepmc +1 more source
Chemical and genetic knockout identifies KCNQ2 as the principal background voltage-gated potassium current in human embryonic kidney 293 cells. [PDF]
O'Neill MJ +4 more
europepmc +1 more source
Early Onset Memory Deficit of WMI Rats Compared to Their Nearly Isogenic WLIs Is Reversed by Enriched Environment in Females. [PDF]
Ji MT +9 more
europepmc +1 more source
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine. [PDF]
Glazer AM +15 more
europepmc +1 more source

