TY  - GEN
AU  - Fratter,C
AU  - Gorman,G S
AU  - Stewart,J D
AU  - Buddles,M
AU  - Smith,C
AU  - Evans,J
AU  - Seller,A
AU  - Poulton,J
AU  - Roberts,M
AU  - Hanna,M G
AU  - Rahman,S
AU  - Omer,S E
AU  - Klopstock,T
AU  - Schoser,B
AU  - Kornblum,C
AU  - Czermin,B
AU  - Lecky,B
AU  - Blakely,E L
AU  - Craig,K
AU  - Chinnery,P F
AU  - Turnbull,D M
AU  - Horvath,R
AU  - Taylor,R W
TI  - The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO
SN  - 1526-632X
PY  - 2010///0602
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Child
KW  - DNA Helicases
KW  - genetics
KW  - DNA, Mitochondrial
KW  - Female
KW  - Genetic Association Studies
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mitochondria, Muscle
KW  - Mitochondrial Proteins
KW  - Muscle, Skeletal
KW  - pathology
KW  - Mutation
KW  - Oculomotor Muscles
KW  - Ophthalmoplegia, Chronic Progressive External
KW  - Phenotype
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1212/WNL.0b013e3181df099f
ER  -