TY  - GEN
AU  - Yu,C E
AU  - Oshima,J
AU  - Wijsman,E M
AU  - Nakura,J
AU  - Miki,T
AU  - Piussan,C
AU  - Matthews,S
AU  - Fu,Y H
AU  - Mulligan,J
AU  - Martin,G M
AU  - Schellenberg,G D
TI  - Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group
SN  - 0002-9297
PY  - 1997///0213
KW  - Asian People
KW  - genetics
KW  - Consensus Sequence
KW  - DNA Helicases
KW  - chemistry
KW  - Exodeoxyribonucleases
KW  - Exons
KW  - Frameshift Mutation
KW  - Haplotypes
KW  - Heterozygote
KW  - Humans
KW  - Introns
KW  - Japan
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Phenotype
KW  - Point Mutation
KW  - RecQ Helicases
KW  - Sequence Deletion
KW  - Werner Syndrome
KW  - Werner Syndrome Helicase
KW  - White People
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
ER  -