MITOCHONDRIAL ACETOACETYL COENZYME-A THIOLASE GENE - A NOVEL 68-BP DELETION INVOLVING 3' SPLICE-SITE OF INTRON-7, CAUSING EXON-8 SKIPPING IN A CAUCASIAN PATIENT WITH BETA-KETOTHIOLASE DEFICIENCY

被引:11
作者
FUKAO, T
SONG, XQ
YAMAGUCHI, S
ORII, T
WANDERS, RJA
POLLTHE, BT
HASHIMOTO, T
机构
[1] SHIMANE MED UNIV,DEPT PEDIAT,IZUMO,SHIMANE 693,JAPAN
[2] UNIV HOSP AMSTERDAM,DEPT PEDIAT CLIN LAB,AMSTERDAM,NETHERLANDS
[3] UNIV UTRECHT,CHILDRENS HOSP WILHELMINA KINDERZIEKENHUIS,DEPT METAB DIS,UTRECHT,NETHERLANDS
[4] SHINSHU UNIV,SCH MED,DEPT BIOCHEM,MATSUMOTO,NAGANO 390,JAPAN
关键词
D O I
10.1002/humu.1380050113
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:94 / 96
页数:3
相关论文
共 14 条
[1]   SHORT, DIRECT REPEATS AT THE BREAKPOINTS OF DELETIONS OF THE RETINOBLASTOMA GENE [J].
CANNING, S ;
DRYJA, TP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5044-5048
[2]  
DAUM RS, 1971, LANCET, V2, P1289
[3]   IDENTIFICATION OF 3 MUTANT ALLELES OF THE GENE FOR MITOCHONDRIAL ACETOACETYL-COENZYME-A THIOLASE - A COMPLETE ANALYSIS OF 2 GENERATIONS OF A FAMILY WITH 3-KETOTHIOLASE DEFICIENCY [J].
FUKAO, T ;
YAMAGUCHI, S ;
ORII, T ;
SCHUTGENS, RBH ;
OSUMI, T ;
HASHIMOTO, T .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (02) :474-479
[4]   MOLECULAR STUDIES OF MITOCHONDRIAL ACETOACETYL-COENZYME A THIOLASE DEFICIENCY IN THE 2 ORIGINAL FAMILIES [J].
FUKAO, T ;
YAMAGUCHI, S ;
SCRIVER, CR ;
DUNBAR, G ;
WAKAZONO, A ;
KANO, M ;
ORII, T ;
HASHIMOTO, T .
HUMAN MUTATION, 1993, 2 (03) :214-220
[5]   MOLECULAR-CLONING AND SEQUENCE OF THE COMPLEMENTARY-DNA ENCODING HUMAN MITOCHONDRIAL ACETOACETYL-COENZYME-A THIOLASE AND STUDY OF THE VARIANT ENZYMES IN CULTURED FIBROBLASTS FROM PATIENTS WITH 3-KETOTHIOLASE DEFICIENCY [J].
FUKAO, T ;
YAMAGUCHI, S ;
KANO, M ;
ORII, T ;
FUJIKI, Y ;
OSUMI, T ;
HASHIMOTO, T .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (06) :2086-2092
[6]   IDENTIFICATION OF A NOVEL EXONIC MUTATION AT -13 FROM 5' SPLICE-SITE CAUSING EXON SKIPPING IN A GIRL WITH MITOCHONDRIAL ACETOACETYL-COENZYME-A THIOLASE DEFICIENCY [J].
FUKAO, T ;
YAMAGUCHI, S ;
WAKAZONO, A ;
ORII, T ;
HOGANSON, G ;
HASHIMOTO, T .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :1035-1041
[7]   MOLECULAR-BASIS OF 3-KETOTHIOLASE DEFICIENCY - IDENTIFICATION OF AN AG TO AC SUBSTITUTION AT THE SPLICE ACCEPTOR SITE OF INTRON-10 CAUSING EXON-11 SKIPPING [J].
FUKAO, T ;
YAMAGUCHI, S ;
ORII, T ;
OSUMI, T ;
HASHIMOTO, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1139 (03) :184-188
[8]   EVIDENCE FOR A STRUCTURAL MUTATION (347ALATOTHR) IN A GERMAN FAMILY WITH 3-KETOTHIOLASE DEFICIENCY [J].
FUKAO, T ;
YAMAGUCHI, S ;
TOMATSU, S ;
ORII, T ;
FRAUENDIENSTEGGER, G ;
SCHROD, L ;
OSUMI, T ;
HASHIMOTO, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (01) :124-129
[9]   STRUCTURE AND EXPRESSION OF THE HUMAN MITOCHONDRIAL ACETOACETYL-COA THIOLASE-ENCODING GENE [J].
KANO, M ;
FUKAO, T ;
YAMAGUCHI, S ;
ORII, T ;
OSUMI, T ;
HASHIMOTO, T .
GENE, 1991, 109 (02) :285-290
[10]   CHROMOSOME MAPPING OF THE HUMAN MITOCHONDRIAL ACETOACETYL-COENZYME-A THIOLASE GENE TO 11Q22.3-]Q23.1 BY FLUORESCENCE INSITU HYBRIDIZATION [J].
MASUNO, M ;
KANO, M ;
FUKAO, T ;
YAMAGUCHI, S ;
OSUMI, T ;
HASHIMOTO, T ;
TAKAHASHI, E ;
HORI, T ;
ORII, T .
CYTOGENETICS AND CELL GENETICS, 1992, 60 (02) :121-122