Oshima, J

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