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

Pubmed ID: 
20708716
Year: 
2011
Month: 
JAN
Volume: 
11
Issue: 
1
Citation: 
Compton AG, Troedson C, Wilson M, Procopis PG, Li FY, Brundage EK, Yamazaki T, Thorburn DR, Wong LJ. Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion 11 (1) : 104 - 7(2011) PubMed