发明授权
US5225546A Diagnosis of hereditary retinal degenerative disease 失效
遗传性视网膜退行性疾病诊断

Diagnosis of hereditary retinal degenerative disease
摘要:
A probe/primer which includes a substantially purified single stranded oligonucleotide containing a region the sequence of which is identical to the sequence of a six-nucleotide, single-stranded segment of a gene encoding a mutant form of a human photoreceptor protein, which segment includes the mutation; and methods of making and using such probe/primer.
公开/授权文献
信息查询
0/0