机译:TUBA1A突变引起广谱性脑干(大脑平滑),并提示多个神经元迁移途径在α微管蛋白上汇聚
Department of Human Genetics,;
Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK,;
Department of Human Genetics,;
Institute of Life Science, School of Medicine, Swansea University, Singleton Park SA2 8PP, UK,;
Department of Pharmacology, The School of Pharmacy, London WC1N 1AX, UK,;
Institute of Structural and Molecular Biology, Crystallography, Birkbeck College, University of London, Malet Street, London WC1E 7HX, UK,;
Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, NE1 3BZ, UK,;
The Dubowitz Neuromuscular Centre, Great Ormond Street Hospital, London WC1N 3JN, UK,;
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany and;
Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA Rotterdam, The Netherlands;
Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK,|Institute of Life Science, School of Medicine, Swansea University, Singleton Park SA2 8PP, UK,;
Department of Pharmacology, The School of Pharmacy, London WC1N 1AX, UK,;
机译:TUBA1A突变引起广谱性脑干(大脑光滑),并提示多个神经元迁移途径在α微管蛋白上汇聚。
机译:微管蛋白α1A(TUBA1A)的从头错义突变产生的大范围的lissencephaly和pachygyria表型。
机译:令人留置症患者鉴定的Tuba1A突变占据了神经元迁移和损害Dynein活性的患者
机译:TUBA1A突变引起广谱性脑干(大脑平滑)并提示多个神经元迁移途径在α微管蛋白上汇聚
机译:TUBA1A突变引起广谱性脑干(大脑平滑),并提示多个神经元迁移途径在α微管蛋白上汇聚