TY  - GEN
AU  - Kuhle,S
AU  - Lane,D A
AU  - Jochmanns,K
AU  - Male,C
AU  - Quehenberger,P
AU  - Lechner,K
AU  - Pabinger,I
TI  - Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism
SN  - 0340-6245
PY  - 2002///0502
KW  - Adolescent
KW  - Age of Onset
KW  - Amino Acid Substitution
KW  - Antithrombin III
KW  - chemistry
KW  - Antithrombin III Deficiency
KW  - epidemiology
KW  - Binding Sites
KW  - Brain Ischemia
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Infarction, Middle Cerebral Artery
KW  - Male
KW  - Mutation, Missense
KW  - Point Mutation
KW  - Thromboembolism
KW  - Thrombophilia
KW  - Venous Thrombosis
KW  - Yugoslavia
N1  - Publication Type: Case Reports; Journal Article; Review
ER  -