机译:CLTRN功能的丧失产生神经精神疾病和模拟HARTNUP疾病的生化表型
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Department of Genetics and Molecular Medicine‐IPER Institut de Recerca Sant Joan de Déu and;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Laboratory of Synaptic Metabolism Institut de Recerca Sant Joan de Déu and CIBERER (ISCIII;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Department of Genetics and Molecular Medicine‐IPER Institut de Recerca Sant Joan de Déu and;
Department of Genetics and Molecular Medicine‐IPER Institut de Recerca Sant Joan de Déu and;
Department of Genetics and Molecular Medicine‐IPER Institut de Recerca Sant Joan de Déu and;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
Department of Clinical Biochemistry Institut de Recerca Sant Joan de Déu and CIBERER (ISCIII;
Laboratory of Synaptic Metabolism Institut de Recerca Sant Joan de Déu and CIBERER (ISCIII;
Department of Molecular and Human GeneticsBaylor College of MedicineHouston Texas;
aminoaciduria; B 0 AT1; CLTRN; EAAC1; Hartnup disease; rBAT‐b 0; + AT;
机译:CLTRN功能的丧失产生神经精神疾病和模拟HARTNUP疾病的生化表型
机译:CLTRN功能的丧失产生神经精神疾病和模拟HARTNUP疾病的生化表型
机译:CRISPR工程化的镶嵌技术迅速揭示了小鼠 Kcnj13 i>功能的丧失模仿了人类疾病的表型
机译:16.血管巨噬细胞表型:肺病中的适应性编程和疾病
机译:神经精神疾病关联研究中的混杂因素:双相情感障碍的个案研究
机译:勘误表:CRISPR工程化的镶嵌技术迅速揭示出小鼠中Kcnj13功能的丧失模仿了人类疾病的表型
机译:Nomo1基因的功能丧失会导致神经精神障碍相关的表型