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机译:适配器蛋白质复合物4缺乏:由缺陷蛋白质贩运引起的儿童发病遗传痉挛截瘫的范式
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Univ Cambridge Cambridge Inst Med Res Cambridge CB2 0XY England;
Univ Sheffield Sheffield Inst Translat Neurosci SITraN Dept Neurosci Sheffield S10 2HQ S;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp Translat Neurosci Ctr Boston MA 02115 USA;
Harvard Med Sch Boston Childrens Hosp Translat Neurosci Ctr Boston MA 02115 USA;
Harvard Med Sch Boston Childrens Hosp Translat Neurosci Ctr Boston MA 02115 USA;
Harvard Med Sch Boston Childrens Hosp Translat Neurosci Ctr Boston MA 02115 USA;
Harvard Med Sch Boston Childrens Hosp Translat Neurosci Ctr Boston MA 02115 USA;
Univ Cambridge Cambridge Inst Med Res Cambridge CB2 0XY England;
Friedrich Alexander Univ Erlangen Nurnberg Inst Human Genet D-91054 Erlangen Germany;
Weill Cornell Med Dept Pediat Div Pediat Neurol New York NY 10021 USA;
IRCCS E Medea Sci Inst Unita Operat Conegliano I-31015 Treviso Italy;
Ctr Hosp Lisboa Cent Dept Pediat Neurol P-1169050 Lisbon Portugal;
Univ Washington Dept Pediat Div Genet Med Seattle WA 98195 USA;
UCL Inst Neurol Dept Mol Neurosci London WC1E 6BT England;
UCL Inst Neurol Dept Mol Neurosci London WC1E 6BT England;
CHU Montpellier Pediat Neurol F-34295 Montpellier France;
IRCCS Fdn Stella Maris Mol Med I-56018 Pisa Italy;
Univ Cambridge Cambridge Inst Med Res Cambridge CB2 0XY England;
Univ Sheffield Sheffield Inst Translat Neurosci SITraN Dept Neurosci Sheffield S10 2HQ S;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Max Planck Inst Biochem Dept Prote &
Signal Transduct D-82152 Martinsried Germany;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
Harvard Med Sch Boston Childrens Hosp FM Kirby Neurobiol Ctr Dept Neurol 3 Blackfan Circle CLSB;
机译:适配器蛋白质复合物4缺乏:由缺陷蛋白质贩运引起的儿童发病遗传痉挛截瘫的范式
机译:定义衔接蛋白复合物4相关遗传性痉挛性截瘫患者的临床,分子和影像谱
机译:衔接蛋白复合物4缺乏会导致严重的常染色体隐性智力障碍,进行性痉挛性截瘫,性格害羞和身材矮小。
机译:可视化蛋白质贩运:膜蛋白遵循极化上皮细胞中基底外侧细胞表面的多种贩运途径。
机译:果蝇突变M1 Spastin在遗传性痉挛性截瘫治疗中毒性作用的果蝇模型的开发和操纵。
机译:衔接蛋白复合物4缺乏会导致严重的常染色体隐性遗传性智力障碍进行性痉挛性截瘫性格害羞和身材矮小
机译:适配器蛋白复合物AP-4和AP-5:内体贩运和进步痉挛性截瘫的新玩家