INHERITANCE OF 2 TYPES OF DEFICIENCY OF HUMAN-SERUM CHOLINESTERASE

被引：19

作者：

SCOTT, EM ^{[1
]}

机构：

[1] DEPT HEW,ARCTIC HLTH RES CTR,FAIRBANKS,AK 99701

来源：

ANNALS OF HUMAN GENETICS | 1973年 / 37卷 / OCT期

关键词：

D O I：

10.1111/j.1469-1809.1973.tb01821.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：139 / 143

页数：5

共 12 条

[1] HETEROGENEITY IN SILENT GENE PHENOTYPE OF PSEUDOCHOLINESTERASE OF HUMAN SERUM [J].

ALTLAND, K ;

GOEDDE, HW .

BIOCHEMICAL GENETICS, 1970, 4 (02) :321-&

[2] RESIDUAL ENZYME ACTIVITY IN SERUM OF A HOMOZYGOTE FOR SILENT PSEUDOCHOLINESTERASE GENE [J].

GAFFNEY, PJ ;

LEHMANN, H .

HUMAN HEREDITY, 1969, 19 (03) :234-&

[3] HEREDITARY DEFICIENCY OF PSEUDOCHOLINESTERASE IN ESKIMOS [J].

GUTSCHE, BB ;

SCOTT, EM ;

WRIGHT, RC .

NATURE, 1967, 215 (5098) :322-&

[4]

HEYWORTH E, 1967, LANCET, V2, P1422

[5] COMPLETE PSEUDOCHOLINESTERASE DEFICIENCY - GENETIC AND IMMUNOLOGIC CHARACTERIZATION [J].

HODGKIN, WE ;

GIBLETT, ER ;

LEVINE, H ;

BAUER, W ;

MOTULSKY, AG .

JOURNAL OF CLINICAL INVESTIGATION, 1965, 44 (03) :486-&

[6] A METHOD FOR THE DETECTION OF ATYPICAL FORMS OF HUMAN SERUM CHOLINESTERASE - DETERMINATION OF DIBUCAINE NUMBERS [J].

KALOW, W ;

GENEST, K .

CANADIAN JOURNAL OF BIOCHEMISTRY AND PHYSIOLOGY, 1957, 35 (06) :339-346

[7]

RUBINSTEIN H M, 1970, Journal of Clinical Investigation, V49, P479, DOI 10.1172/JCI106257

[8] PROPERTIES OF TRACE ENZYME IN HUMAN SERUM CHOLINESTERASE DEFICIENCY [J].

SCOTT, EM .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1970, 38 (05) :902-&

[9] ELECTROPHORESIS IN STARCH GEL OF HUMAN SERUM CHOLINESTERASE [J].

SCOTT, EM ;

WEAVER, DD .

BIOCHEMICAL MEDICINE, 1970, 4 (3-4) :349-&

[10]

SCOTT EM, 1970, AM J HUM GENET, V22, P363

← 1 2 →