Detecting single-base mutations.

Abstract:

:The ability to detect single-base changes is of fundamental importance in molecular genetics. This is particularly true in human genetics, where interest in linking mutations of identified genes to particular disease phenotypes is most intense, and where a demand exists for clinical diagnosis of defined mutations. In the following article, techniques are described for screening unknown mutations, as well as diagnosing those that have been identified previously. The underlying methods are explained briefly and guidelines are offered for choosing one technique in preference to another.

journal_name

Trends Biotechnol

journal_title

Trends in biotechnology

authors

Prosser J

doi

10.1016/0167-7799(93)90135-V

subject

Has Abstract

pub_date

1993-06-01 00:00:00

pages

238-46

issue

6

eissn

0167-7799

issn

1879-3096

pii

0167-7799(93)90135-V

journal_volume

11

pub_type

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