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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
Author(s) -
Menardi Claudia,
Schneider Rainer,
NeuschmidKaspar Felizia,
Klocker Helmut,
HirschKauffmann Monica,
Auer Bernhard,
Schweiger Manfred
Publication year - 1997
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1997)10:3<251::aid-humu15>3.0.co;2-z
Subject(s) - medicine