TY  - GEN
AU  - Jayandharan,G
AU  - Viswabandya,A
AU  - Baidya,S
AU  - Nair,S C
AU  - Shaji,R V
AU  - George,B
AU  - Chandy,M
AU  - Srivastava,A
TI  - Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin
SN  - 1538-7933
PY  - 2005///0927
KW  - Arginine
KW  - chemistry
KW  - Codon, Nonsense
KW  - CpG Islands
KW  - DNA Mutational Analysis
KW  - DNA Primers
KW  - Epitopes
KW  - Exons
KW  - Factor Va
KW  - Factor X
KW  - genetics
KW  - Factor X Deficiency
KW  - diagnosis
KW  - Frameshift Mutation
KW  - Heterozygote
KW  - Humans
KW  - India
KW  - Lysine
KW  - Models, Genetic
KW  - Models, Molecular
KW  - Mutation
KW  - Mutation, Missense
KW  - Nepal
KW  - Phenylalanine
KW  - Serine
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1538-7836.2005.01339.x
ER  -