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UnknownEnhancer-gene rewiring in the pathogenesis of Quebec platelet disorder.
Not available
S-EPMC7735161 | biostudies-literature
UnknownEarly-Life Exposure to Environmental Contaminants Perturbs the Sperm Epigenome and Induces Negative Pregnancy Outcomes for Three Generations via the Paternal Lineage.
Not available
S-EPMC8594730 | biostudies-literature
UnknownCompound muscle action potential and motor function in children with spinal muscular atrophy.
Not available
S-EPMC2964439 | biostudies-literature
UnknownSMA valiant trial: a prospective, double-blind, placebo-controlled trial of valproic acid in ambulatory adults with spinal muscular atrophy.
Not available
S-EPMC3888833 | biostudies-literature
UnknownSMA CARNIVAL TRIAL PART II: a prospective, single-armed trial of L-carnitine and valproic acid in ambulatory children with spinal muscular atrophy.
Not available
S-EPMC3130730 | biostudies-literature
UnknownSMA CARNI-VAL trial part I: double-blind, randomized, placebo-controlled trial of L-carnitine and valproic acid in spinal muscular atrophy.
Not available
S-EPMC2924376 | biostudies-literature
UnknownExpanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Not available
S-EPMC6323608 | biostudies-literature
UnknownThe MOG antibody non-P42 epitope is predictive of a relapsing course in MOG antibody-associated disease.
Not available
S-EPMC11103329 | biostudies-literature
UnknownCHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476 | biostudies-literature
UnknownGrowth differences between North American and European children at risk for type 1 diabetes.
Not available
S-EPMC3335929 | biostudies-literature
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