TY  - GEN
AU  - Pung-amritt,P
AU  - Poort,S R
AU  - Vos,H L
AU  - Bertina,R M
AU  - Mahasandana,C
AU  - Tanphaichitr,V S
AU  - Veerakul,G
AU  - Kankirawatana,S
AU  - Suvatte,V
TI  - Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency
SN  - 0340-6245
PY  - 1999///0604
KW  - Alleles
KW  - Blindness
KW  - etiology
KW  - Codon
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Disseminated Intravascular Coagulation
KW  - Endophthalmitis
KW  - Exons
KW  - Female
KW  - Fetal Diseases
KW  - Gene Frequency
KW  - Genetic Predisposition to Disease
KW  - Heterozygote
KW  - Humans
KW  - IgA Vasculitis
KW  - congenital
KW  - Infant, Newborn
KW  - Point Mutation
KW  - Protein S
KW  - Protein S Deficiency
KW  - complications
KW  - Retinal Vein Occlusion
KW  - embryology
KW  - Risk Factors
KW  - Thailand
KW  - Thrombophilia
KW  - epidemiology
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
ER  -