HEREDITARY HEPATIC PORPHYRIA WITH DELTA-AMINOLEVULINATE DEHYDRASE DEFICIENCY - IMMUNOLOGICAL CHARACTERIZATION OF THE NON-CATALYTIC ENZYME

被引：24

作者：

DEVERNEUIL, H ^{[1
]}

DOSS, M ^{[1
]}

BRUSCO, N ^{[1
]}

BEAUMONT, C ^{[1
]}

NORDMANN, Y ^{[1
]}

机构：

[1] UNIV MARBURG,FAC MED,D-3550 MARBURG,FED REP GER

来源：

HUMAN GENETICS | 1985年 / 69卷 / 02期

关键词：

D O I：

10.1007/BF00293292

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：174 / 177

页数：4

共 22 条

[1]

ANDERSON PM, 1979, J BIOL CHEM, V254, P6924

[2] CHARACTERIZATION OF THE PORPHOBILINOGEN DEAMINASE DEFICIENCY IN ACUTE INTERMITTENT PORPHYRIA - IMMUNOLOGICAL EVIDENCE FOR HETEROGENEITY OF THE GENETIC-DEFECT [J].

ANDERSON, PM ;

REDDY, RM ;

ANDERSON, KE ;

DESNICK, RJ .

JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (01) :1-12

[3] PEROXIDASE LABELLED ANTIBODY AND FAB CONJUGATES WITH ENHANCED INTRACELLULAR PENETRATION [J].

AVRAMEAS, S ;

TERNYNCK, T .

IMMUNOCHEMISTRY, 1971, 8 (12) :1175-&

[4] DELTA-AMINOLEVULINATE DEHYDRASE - A NEW GENETIC-POLYMORPHISM IN MAN [J].

BATTISTUZZI, G ;

PETRUCCI, R ;

SILVAGNI, L ;

URBANI, FR ;

CAIOLA, S .

ANNALS OF HUMAN GENETICS, 1981, 45 (JUL) :223-229

[5] ASSIGNMENT OF THE HUMAN-GENE FOR DELTA-AMINOLEVULINATE DEHYDRASE TO CHROMOSOME-9 BY SOMATIC-CELL HYBRIDIZATION AND SPECIFIC ENZYME-IMMUNOASSAY [J].

BEAUMONT, C ;

FOUBERT, C ;

GRANDCHAMP, B ;

WEIL, D ;

NGUYEN, VC ;

GROSS, MS ;

NORDMANN, Y .

ANNALS OF HUMAN GENETICS, 1984, 48 (MAY) :153-159

[6] POLYMORPHISM OF DELTA-AMINOLEVULINIC-ACID DEHYDRATASE IN VARIOUS POPULATIONS [J].

BENKMANN, HG ;

BOGDANSKI, P ;

GOEDDE, HW .

HUMAN HEREDITY, 1983, 33 (01) :62-64

[7]

BIRD TD, 1979, AM J HUM GENET, V31, P662

[8] HEREDITARY PORPHOBILINOGEN SYNTHASE DEFICIENCY IN HUMAN ASSOCIATED WITH ACUTE HEPATIC PORPHYRIA [J].

BRANDT, A ;

DOSS, M .

HUMAN GENETICS, 1981, 58 (02) :194-197

[9]

DESASSA S, UNPUB T ASS AM PHYSI

[10]

DESPAUX N, 1979, BIOCHIMIE, V61, P1021

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