机译:影响Tourette综合征患者IMMP2L基因的两种替代转录物的腺体缺失
Applied Human Molecular Genetics Kennedy Center Copenhagen University HospitalGlostrup Denmark;
Applied Human Molecular Genetics Kennedy Center Copenhagen University HospitalGlostrup Denmark;
Institute for Human Genetics Ernst-Moritz-Arndt-University GreifswaldGriefswald Germany;
Tourette Clinic Department of Pediatrics Herlev University HospitalHerlev Denmark;
Center for Neuropsychiatric Schizophrenia Research Center for Clinical Intervention and;
Section of Child Neuropsychiatry Department of Pediatrics University of CataniaCatania Italy;
Tourette Clinic Department of Pediatrics Herlev University HospitalHerlev Denmark;
Tourette Clinic Department of Pediatrics Herlev University HospitalHerlev Denmark;
Applied Human Molecular Genetics Kennedy Center Copenhagen University HospitalGlostrup Denmark;
Department of Molecular Biology and Genetics Democritus University of ThraceAlexandroupoli Greece;
Institute for Cellular and Molecular Medicine University of CopenhagenCopenhagen Denmark;
Applied Human Molecular Genetics Kennedy Center Copenhagen University HospitalGlostrup Denmark;
ADHD; IMMP2L; intronic deletions; OCD; susceptibility gene; Tourette syndrome;
机译:内源性缺失会影响Tourette综合征患者IMMP2L基因的两个替代转录本
机译:在Gilles de la Tourette综合征患者的线粒体功能患者,无腺瘤<斜视> Immp2L 斜体>缺失
机译:同时患有吉尔·德·图雷特氏综合症和22q11号染色体缺失综合症的患者:吉列斯·图雷特氏综合症的遗传学线索?
机译:22Q11.2缺失综合征在调查白质改变的替代扩散各向异性措施
机译:控制吉尔斯·德·图雷特综合症患者的抽搐发作并改善其生活质量:是否存在药物治疗以外的替代方法?
机译:内源性缺失影响图雷特综合征患者IMMP2L基因的两个替代转录本
机译:LHX6,IMMP2L和AADAC与Tourette综合征的遗传变异结合