IDENTIFICATION OF VARIANT ALPORT PHENOTYPES USING AN ALPORT-SPECIFIC ANTIBODY PROBE

被引:38
作者
KASHTAN, CE
ATKIN, CL
GREGORY, MC
MICHAEL, AF
机构
[1] UNIV UTAH,MED CTR,DEPT BIOCHEM,SALT LAKE CITY,UT 84112
[2] UNIV UTAH,MED CTR,DEPT MED,SALT LAKE CITY,UT 84112
关键词
D O I
10.1038/ki.1989.244
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:669 / 674
页数:6
相关论文
共 44 条
[1]  
ATKIN CL, 1988, AM J HUM GENET, V42, P249
[2]  
BOYD CD, 1988, AM J HUM GENET, V42, P309
[3]   THE SINGLE COPY GENE CODING FOR HUMAN ALPHA-1(IV) PROCOLLAGEN IS LOCATED AT THE TERMINAL END OF THE LONG ARM OF CHROMOSOME-13 [J].
BOYD, CD ;
WELIKY, K ;
TOTHFEJEL, SE ;
DEAK, SB ;
CHRISTIANO, AM ;
MACKENZIE, JW ;
SANDELL, LJ ;
TRYGGVASON, K ;
MAGENIS, E .
HUMAN GENETICS, 1986, 74 (02) :121-125
[4]  
BUTKOWSKI RJ, 1987, J BIOL CHEM, V262, P7874
[5]   HEREDITARY NEPHRITIS - CLINICAL SPECTRUM AND MODE OF INHERITANCE IN 5 NEW KINDREDS [J].
CHAZAN, JA ;
ZACKS, J ;
COHEN, JJ ;
GARELLA, S .
AMERICAN JOURNAL OF MEDICINE, 1971, 50 (06) :764-+
[6]  
CHURG J, 1973, ARCH PATHOL, V95, P374
[7]  
CRAWFURD MD, 1988, GENETICS RENAL TRACT, P306
[8]  
EMANUEL BS, 1986, AM J HUM GENET, V38, P38
[9]   HEREDITARY MACROTHROMBOCYTOPATHIA, NEPHRITIS AND DEAFNESS [J].
EPSTEIN, CJ ;
SAHUD, MA ;
GOODMAN, JR ;
ABLIN, AR ;
BERNFIELD, MR ;
PIEL, CF ;
KUSHNER, JH .
AMERICAN JOURNAL OF MEDICINE, 1972, 52 (03) :299-+
[10]  
EVANS SH, 1980, CLIN GENET, V17, P285