首页> 外国专利> methods for detecting an exel 9 deletion mutation in the calreticulin gene exon 9, for diagnosing a hematopoietic disease in a patient, for determining the likelihood of a patient developing a mutation in a jak-stat pathway gene to determine the prognosis of a patient with a myeloproliferative disease, kit, and oligonucleotide probe or primer

methods for detecting an exel 9 deletion mutation in the calreticulin gene exon 9, for diagnosing a hematopoietic disease in a patient, for determining the likelihood of a patient developing a mutation in a jak-stat pathway gene to determine the prognosis of a patient with a myeloproliferative disease, kit, and oligonucleotide probe or primer

机译:用于检测钙网蛋白基因外显子9中exel 9缺失突变的方法,用于诊断患者的造血系统疾病,确定患者发生jak-stat通路基因突变的可能性,从而确定患者的预后骨髓增生性疾病,试剂盒和寡核苷酸探针或引物

摘要

provided herein are methods and compositions for detecting deletion germline mutations in the calr gene. Methods are also provided to determine the prognosis of myeloproliferative diseases and the likelihood of developing somatic mutations in genes involved in the jak-stat pathway.
机译:本文提供了用于检测calr基因中缺失种系突变的方法和组合物。还提供了确定骨髓增生性疾病的预后以及在jak-stat途径中涉及的基因中发生体细胞突变的可能性的方法。

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