TY  - GEN
AU  - Arbini,A A
AU  - Mannucci,M
AU  - Bauer,K A
TI  - A Thr359Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule
SN  - 0006-4971
PY  - 1996///0731
KW  - Adult
KW  - Alleles
KW  - Animals
KW  - Base Sequence
KW  - CHO Cells
KW  - Carrier Proteins
KW  - metabolism
KW  - Cloning, Molecular
KW  - Codon
KW  - genetics
KW  - Cricetinae
KW  - Cricetulus
KW  - DNA Mutational Analysis
KW  - DNA, Complementary
KW  - Endoplasmic Reticulum
KW  - Endoplasmic Reticulum Chaperone BiP
KW  - Factor VII
KW  - chemistry
KW  - Factor VII Deficiency
KW  - Female
KW  - Glycosylation
KW  - Heat-Shock Proteins
KW  - Humans
KW  - Molecular Chaperones
KW  - Molecular Sequence Data
KW  - Pedigree
KW  - Point Mutation
KW  - Protein Folding
KW  - Protein Processing, Post-Translational
KW  - RNA Splicing
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S
ER  -