POLG mutations associated with Alpers syndrome and mitochondrial DNA depletion

被引：40

作者：

Naviaux, RK

Nguyen, KV

机构：

来源：

关键词：

D O I：

10.1002/ana.20544

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：491 / 491

页数：1

共 4 条

[1] POLG mutations and Alpers syndrome
Davidzon, G
Mancuso, M
Ferraris, S
Quinzii, C
Hirano, M
Peters, HL
Kirby, D
Thorburn, DR
DiMauro, S
[J]. ANNALS OF NEUROLOGY, 2005, 57 (06) : 921 - 923
[2] Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-γA
Ferrari, G
Lamantea, E
Donati, A
Filosto, M
Briem, E
Carrara, F
Parini, R
Simonati, A
Santer, R
Zeviani, M
[J]. BRAIN, 2005, 128 : 723 - 731
[3] POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
Naviaux, RK
Nguyen, KV
[J]. ANNALS OF NEUROLOGY, 2004, 55 (05) : 706 - 712
[4] *NIEHS, 2005, GEN SNPS POLG