Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome

Saved in:
Bibliographic Details
Title: Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome
Authors: Compton, Alison G.1, Troedson, Christopher2, Wilson, Meredith3, Procopis, Peter G.2, Li, Fang-Yuan4, Brundage, Ellen K.4, Yamazaki, Taro1,5, Thorburn, David R.1,6 david.thorburn@mcri.edu.au, Wong, Lee-Jun C.4
Source: Mitochondrion. Jan2011, Vol. 11 Issue 1, p104-107. 4p.
Database: Academic Search Ultimate
Description
ISSN:15677249
DOI:10.1016/j.mito.2010.07.012