INVESTIGATIONS ON PGM1A POLYMORPHISM (PHOSPHOGLUCOMUTASE-EC-2.7.5.1) BY ISOELECTRIC-FOCUSING

被引:62
作者
KUHNL, P
SPIELMANN, W
机构
关键词
D O I
10.1007/BF00396479
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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页码:57 / 67
页数:11
相关论文
共 18 条
[1]  
[Anonymous], 1976, HDB ENZYME ELECTROPH
[2]  
ARNAUD P, 1975, LKB185 APPL NOT
[3]   TYPING OF COMMON PHOSPHOGLUCOMUTASE VARIANTS USING ISOELECTRIC-FOCUSING - NEW INTERPRETATION OF PHOSPHOGLUCOMUTASE SYSTEM [J].
BARK, JE ;
HARRIS, MJ ;
FIRTH, M .
JOURNAL OF THE FORENSIC SCIENCE SOCIETY, 1976, 16 (02) :115-120
[4]  
BEUTLER E, 1975, BLOOD, V46, P103
[5]   INHERITED PARTIAL DEFICIENCY OF PGM1/1 GENE - BIOCHEMICAL AND DENSITOMETRIC STUDIES [J].
BRINKMANN, B ;
RUDIGER, HW ;
KOOPS, E ;
HEINDL, K ;
KLOPP, O .
ANNALS OF HUMAN GENETICS, 1972, 35 (MAR) :363-+
[6]   SECONDARY ISOENZYMES DERIVED FROM 3 PGM LOCI [J].
FISHER, RA ;
HARRIS, H .
ANNALS OF HUMAN GENETICS, 1972, 36 (JUL) :69-&
[7]   ALTERED ELECTROPHORETIC MOBILITY OF OXIDIZED PHOSPHOGLUCOMUTASE [J].
GREENE, JM ;
DAWSON, DM .
ANNALS OF HUMAN GENETICS, 1973, 36 (JAN) :355-361
[8]   EVIDENCE FOR 2 ADDITIONAL COMMON ALLELES AT PGM1 LOCUS (PHOSPHOGLUCOMUTASE-EC=2.7.5.1) - COMPARISON BY 3 DIFFERENT TECHNIQUES [J].
KUHNL, P ;
SCHMIDTMANN, U ;
SPIELMANN, W .
HUMAN GENETICS, 1977, 35 (02) :219-223
[9]  
KUHNL P, 1977, ARZTL LAB, V23, P229
[10]  
KUHNL P, 1977, 7TH INT C SOC FOR HA