TY  - GEN
AU  - Gerth,Christina
AU  - Morel,Chantal F
AU  - Feigenbaum,Annette
AU  - Levin,Alex V
TI  - Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type
SN  - 1528-3933
PY  - 2009///0406
KW  - Adolescent
KW  - Age of Onset
KW  - Anterior Eye Segment
KW  - pathology
KW  - Carrier Proteins
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Disease Progression
KW  - Electroretinography
KW  - Eye
KW  - Female
KW  - Fundus Oculi
KW  - Genes, Recessive
KW  - Heterozygote
KW  - Homocystinuria
KW  - classification
KW  - Humans
KW  - Infant
KW  - Longitudinal Studies
KW  - Male
KW  - Metabolism, Inborn Errors
KW  - Methylmalonic Acid
KW  - urine
KW  - Mutation
KW  - Oxidoreductases
KW  - Phenotype
KW  - Retina
KW  - Retinal Diseases
KW  - etiology
KW  - Visual Acuity
KW  - Vitamin B 12
KW  - metabolism
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.jaapos.2008.06.008
ER  -