TY  - GEN
AU  - Meins,M
AU  - Brockmann,K
AU  - Yadav,S
AU  - Haupt,M
AU  - Sperner,J
AU  - Stephani,U
AU  - Hanefeld,F
TI  - Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients
SN  - 0174-304X
PY  - 2002///1113
KW  - Alexander Disease
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Glial Fibrillary Acidic Protein
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Mutation
KW  - Prognosis
KW  - Twins, Monozygotic
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1055/s-2002-34495
ER  -