![](/img/cover-not-exists.png)
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients withUSH2Amonoallelic mutations on Sanger sequencing
Heather B Steele-Stallard,Polona Le Quesne Stabej…Volume:
8
Language:
english
DOI:
10.1186/1750-1172-8-122
Date:
December, 2013
File:
PDF, 336 KB
english, 2013