Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study

被引：78

作者：

Gabolde, M ^{[1
]}

Guilloud-Bataille, M ^{[1
]}

Feingold, J ^{[1
]}

Besmond, C ^{[1
]}

机构：

[1] Hop Robert Debre, INSERM, U458, F-75019 Paris, France

来源：

BRITISH MEDICAL JOURNAL | 1999年 / 319卷 / 7218期

关键词：

D O I：

10.1136/bmj.319.7218.1166

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1166 / 1167

页数：2

共 6 条

[1]

Gabolde M, 1999, HUM MUTAT, V14, P80, DOI 10.1002/(SICI)1098-1004(1999)14:1<80::AID-HUMU10>3.0.CO

[2]

2-J

[3] INCREASED FREQUENCY OF HOMOZYGOSITY OF ABNORMAL MANNAN-BINDING-PROTEIN ALLELES IN PATIENTS WITH SUSPECTED IMMUNODEFICIENCY [J].

GARRED, P ;

MADSEN, HO ;

HOFMANN, B ;

SVEJGAARD, A .

LANCET, 1995, 346 (8980) :941-943

[4] Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis [J].

Hull, J ;

Thomson, AH .

THORAX, 1998, 53 (12) :1018-1021

[5] MOLECULAR-BASIS OF OPSONIC DEFECT IN IMMUNODEFICIENT CHILDREN [J].

SUMIYA, M ;

SUPER, M ;

TABONA, P ;

LEVINSKY, RJ ;

ARAI, T ;

TURNER, MW ;

SUMMERFIELD, JA .

LANCET, 1991, 337 (8757) :1569-1570

[6] MANNOSE-BINDING PROTEIN GENE-MUTATIONS ASSOCIATED WITH UNUSUAL AND SEVERE INFECTIONS IN ADULTS [J].

SUMMERFIELD, JA ;

RYDER, S ;

SUMIYA, M ;

THURSZ, M ;

GORCHEIN, A ;

MONTEIL, MA ;

TURNER, MW .

LANCET, 1995, 345 (8954) :886-889

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