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机译:肌肉磷素(Pygm)突变(Pygm)突变由来自土耳其疾病的土耳其队列中的下一代测序测定
Department of Molecular Medicine Istanbul University Aziz Sancar Institute of Experimental;
Department of Molecular Medicine Istanbul University Aziz Sancar Institute of Experimental;
The Scientific and Technological Research Council of Turkey (TUBITAK) Advanced Genomics and;
Department of Neurology Istanbul University Istanbul Medical Faculty;
Department of Neurology Istanbul University Istanbul Medical Faculty;
The Scientific and Technological Research Council of Turkey (TUBITAK) Advanced Genomics and;
The Scientific and Technological Research Council of Turkey (TUBITAK) Advanced Genomics and;
The Scientific and Technological Research Council of Turkey (TUBITAK) Advanced Genomics and;
Department of Neurology Istanbul University Istanbul Medical Faculty;
Department of Neurology Istanbul University Istanbul Medical Faculty;
Department of Molecular Medicine Istanbul University Aziz Sancar Institute of Experimental;
Department of Molecular Medicine Istanbul University Aziz Sancar Institute of Experimental;
Department of Neurology Hacettepe University School of Medicine;
Department of Neurology Hacettepe University School of Medicine;
Department of Neurology Hacettepe University School of Medicine;
Department of Genetics Istanbul University Aziz Sancar Institute of Experimental Medicine;
Section of Medical Genetics University of Pennsylvania;
Department of Molecular Medicine Istanbul University Aziz Sancar Institute of Experimental;
Department of Neurology Istanbul University Istanbul Medical Faculty;
Glycogenosis; Population specific; Novel mutation; Rare muscle disorders; Molecular screening; Genomics;
机译:肌肉磷素(Pygm)突变(Pygm)突变由来自土耳其疾病的土耳其队列中的下一代测序测定
机译:下一代测序揭示了中国中枢核心疾病队列中的ryanodine受体1突变
机译:下一代测序揭示了中国中枢核心疾病队列中的ryanodine受体1突变
机译:在肌钙磷酸化酶缺乏的情况下,光和电子显微镜(糖化酶v或Mcardle疾病)
机译:从下一代测序数据中识别遗传突变的计算方法
机译:下一代队列中来自土耳其患有McArdle病的队列中确定的肌磷酸化酶(PYGM)突变
机译:382 COL7A1突变检测133近亲家族的隐性营养不良表皮细胞差异Blowosa:疾病靶向下一代测序面板对比较的比较传统的Sanger测序