HOMOZYGOSITY FOR THE ASN187 GELSOLIN MUTATION IN FINNISH-TYPE FAMILIAL AMYLOIDOSIS IS ASSOCIATED WITH SEVERE RENAL-DISEASE

被引：56

作者：

MAURY, CPJ ^{[1
]}

KERE, J ^{[1
]}

TOLVANEN, R ^{[1
]}

DELACHAPELLE, A ^{[1
]}

机构：

[1] UNIV HELSINKI,DEPT MED GENET,SF-00170 HELSINKI 17,FINLAND

来源：

GENOMICS | 1992年 / 13卷 / 03期

基金：

芬兰科学院;

关键词：

D O I：

10.1016/0888-7543(92)90183-S

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

[No abstract available]

引用

页码：902 / 903

页数：2

共 11 条

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[5] GELSOLIN-RELATED AMYLOIDOSIS - IDENTIFICATION OF THE AMYLOID PROTEIN IN FINNISH HEREDITARY AMYLOIDOSIS AS A FRAGMENT OF VARIANT GELSOLIN [J].

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[6] ISOLATION AND CHARACTERIZATION OF CARDIAC AMYLOID IN FAMILIAL AMYLOID POLYNEUROPATHY TYPE-IV (FINNISH) - RELATION OF THE AMYLOID PROTEIN TO VARIANT GELSOLIN [J].

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[7] FINNISH HEREDITARY AMYLOIDOSIS IS CAUSED BY A SINGLE NUCLEOTIDE SUBSTITUTION IN THE GELSOLIN GENE [J].

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FEBS LETTERS, 1990, 276 (1-2) :75-77

[8] FINNISH HEREDITARY AMYLOIDOSIS - AMINO-ACID-SEQUENCE HOMOLOGY BETWEEN THE AMYLOID FIBRIL PROTEIN AND HUMAN PLASMA GELSOLINE [J].

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[9]

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[10]

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