首页> 外国专利> NUCLEIC SEQUENCE OF THE GENE ASSOCIATED WITH X-LINKED KALLMANN SYNDROME CORRESPONDING PEPTIDE SEQUENCES, DIAGNOSTIC APPLICATIONS

NUCLEIC SEQUENCE OF THE GENE ASSOCIATED WITH X-LINKED KALLMANN SYNDROME CORRESPONDING PEPTIDE SEQUENCES, DIAGNOSTIC APPLICATIONS

机译:与X-连锁卡尔曼综合征相应的肽序列相关的基因的核酸序列,在诊断中的应用

摘要

the invention relates to a nucleic acid fragment, which is characterized in that it comprises a nucleotide sequence selected from: (a) seq id no.1. (b) the sequences that differ by mutation, insertion, deletion or substitution of one or more databases; (c) fragments of sequences (a) and (b).(d) the complementary sequences of the sequences (a), (b) and (c); and (e) sequences that hybridize with sequences (a), (b) and (c), and the corresponding amino acid sequence.a fragment of a nucleic acid according to the invention can be used as a primer or probe, in particular to a method for diagnosing a genetic abnormality associated with kallman syndrome.
机译:本发明涉及核酸片段,其特征在于其包含选自以下的核苷酸序列:(a)SEQ ID NO.1。 (b)因一个或多个数据库的突变,插入,缺失或替代而不同的序列; (c)序列(a)和(b)的片段。(d)序列(a),(b)和(c)的互补序列; (e)与序列(a),(b)和(c)杂交的序列以及相应的氨基酸序列。根据本发明的核酸的片段可以用作引物或探针,特别是用于一种诊断与卡尔曼综合症有关的遗传异常的方法。

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