THE FAMILIAL HYPERCHYLOMICRONEMIA SYNDROME - NEW INSIGHTS INTO UNDERLYING GENETIC-DEFECTS

被引：55

作者：

SANTAMARINAFOJO, S

BREWER, HB

机构：

来源：

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1991年 / 265卷 / 07期

关键词：

D O I：

10.1001/jama.265.7.904

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：904 / 908

页数：5

共 34 条

[11] IDENTIFICATION OF THE MUTATION RESPONSIBLE FOR A CASE OF PLASMATIC APOLIPOPROTEIN-CII DEFICIENCY (APO CII-BARI) [J].

CRECCHIO, C ;

CAPURSO, A ;

PEPE, G .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (03) :1118-1127

[12]

DEVLIN RH, 1990, AM J HUM GENET, V46, P112

[13]

DICHEK HL, 1991, J BIOL CHEM, V266, P473

[14]

EMI M, 1990, J BIOL CHEM, V265, P5910

[15]

EMI M, 1990, AM J HUM GENET, V47, P107

[16] SUPPRESSION OF AMYLASE ACTIVITY BY HYPERTRIGLYCERIDEMIA [J].

FALLAT, RW ;

VESTER, JW ;

GLUECK, CJ .

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1973, 225 (11) :1331-1334

[17] A NONSENSE MUTATION IN THE APOLIPOPROTEIN C-IIPADOVA GENE IN A PATIENT WITH APOLIPOPROTEIN C-II DEFICIENCY [J].

FOJO, SS ;

LOHSE, P ;

PARROTT, C ;

BAGGIO, G ;

GABELLI, C ;

THOMAS, F ;

HOFFMAN, J ;

BREWER, HB .

JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1215-1219

[18] DONOR SPLICE SITE MUTATION IN THE APOLIPOPROTEIN (APO) C-II GENE (APO C-II HAMBURG) OF A PATIENT WITH APO C-II DEFICIENCY [J].

FOJO, SS ;

BEISIEGEL, U ;

BEIL, U ;

HIGUCHI, K ;

BOJANOVSKI, M ;

GREGG, RE ;

GRETEN, H ;

BREWER, HB .

JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (05) :1489-1494

[19]

FOJO SS, 1989, J BIOL CHEM, V264, P20839

[20]

FOJO SS, 1988, J BIOL CHEM, V263, P17913

← 1 2 3 4 →