机译:破坏MET转录的遗传变异与自闭症相关
Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37203 USA;
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37203 USA;
Vanderbilt Univ, Vanderbilt Kennedy Ctr Res Human Dev, Nashville, TN 37203 USA;
Univ Naples, Dept Child Neuropsychiat, I-80131 Naples, Italy;
Assoc Anni Verdi ONLUS, I-00148 Rome, Italy;
IRCCS, Sci Inst Res Hospitalizat & Hlth Care, Unit Neurol & Clin Neurophysiopathol, I-94018 Troina, Italy;
SW Autism Res & Resource Ctr, Phoenix, AZ 85006 USA;
Ctr Autism Res & Ecuc, Phoenix, AZ 85012 USA;
Univ Rome, Lab Mol Psychiat Neurogenet, I-00155 Rome, Italy;
IRCCS Fdn Santa Lucia, I-00179 Rome, Italy;
autism spectrum disorder; association; candidate gene; hepatocyte growth factor; hepatocyte growth factor receptor; HEPATOCYTE GROWTH-FACTOR; INFLAMMATORY-BOWEL-DISEASE; GASTROINTESTINAL SYMPTOMS; INTERNEURON DEVELOPMENT; SUSCEPTIBILITY LOCUS; SPECTRUM DISORDERS; MUCOSAL REPAIR; PHENOTYPE; HAPLOTYPES; MONOCYTES;
机译:令人惊讶的MET畸变:自闭症遗传学发现一种常见的功能变异
机译:DNMT变体的遗传关联可以在定义自闭症中的甲基化模式方面发挥关键作用
机译:在泰国自闭症谱系障碍儿童和青少年中检测到的药物代谢酶和转运蛋白基因的临床相关遗传变异
机译:自闭症男孩的遗传变异分析:将面部表型与基因型联系起来的初步研究
机译:非编码遗传变异在促甲肾上腺素淀粉样蛋白症中的Transthyretin基因转录中的作用
机译:从封面开始:破坏MET转录的遗传变异与自闭症相关
机译:破坏MET转录的遗传变异与自闭症相关