Homozygous and compound heterozygous mutations at the Werner syndrome locus. [electronic resource]
- Human molecular genetics Dec 1996
- 1909-13 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0964-6906
10.1093/hmg/5.12.1909 doi
Asian People DNA Helicases--genetics Exodeoxyribonucleases Heterozygote Homozygote Humans Mutation RecQ Helicases Werner Syndrome--genetics Werner Syndrome Helicase White People