HUMAN APRT DEFICIENCY - INDICATION FOR MULTIPLE ORIGINS OF THE MOST COMMON CAUCASIAN MUTATION AND DETECTION OF A NOVEL TYPE OF MUTATION INVOLVING INTRASTRAND-TEMPLATED REPAIR

Authors
MENARDI C SCHNEIDER R NEUSCHMIDKASPAR F KLOCKER H HIRSCHKAUFFMANN M AUER B SCHWEIGER M
Citation
C. Menardi et al., HUMAN APRT DEFICIENCY - INDICATION FOR MULTIPLE ORIGINS OF THE MOST COMMON CAUCASIAN MUTATION AND DETECTION OF A NOVEL TYPE OF MUTATION INVOLVING INTRASTRAND-TEMPLATED REPAIR, Human mutation, 10(3), 1997, pp. 251-255
Citations number
14
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
10
Issue
3
Year of publication
1997
Pages
251 - 255
Database
ISI
SICI code
1059-7794(1997)10:3<251:HAD-IF>2.0.ZU;2-U