换一批
换一批Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
作者：
主题词
选择性剪接(Alternative Splicing);动物(Animals);碱基序列(Base Sequence);染色体图(Chromosome Mapping);染色体, 人, 22对(Chromosomes, Human, Pair 22);DNA引物(DNA Primers);聋(Deafness);基因成分(Gene Components);基因频率(Gene Frequency);基因, 隐性(Genes, Recessive);人类(Humans);印度(India);小鼠(Mice);微丝蛋白质类(Microfilament Proteins);分子序列数据(Molecular Sequence Data);突变(Mutation);巴基斯坦(Pakistan);系谱(Pedigree);逆转录聚合酶链反应(Reverse Transcriptase Polymerase Chain Reaction);序列分析, DNA(Sequence Analysis, DNA)
DOI
10.1086/499164
PMID
16385457
发布时间
2024-02-27
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