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Volumn 1, Issue 5, 1992, Pages 368-371
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Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
a b c d b b b a |
Author keywords
[No Author keywords available]
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Indexed keywords
LEUCINE TRANSFER RNA;
MITOCHONDRIAL DNA;
OLIGODEOXYRIBONUCLEOTIDE;
RNA;
RNA, MITOCHONDRIAL;
ADULT;
ARTICLE;
CASE REPORT;
CELL CULTURE;
CHILD;
FEMALE;
GENETICS;
HEARING IMPAIRMENT;
HELA CELL;
HETEROZYGOTE DETECTION;
HOMOZYGOTE;
HUMAN;
ISOLATION AND PURIFICATION;
MALE;
METABOLISM;
MOLECULAR GENETICS;
MUSCLE;
NON INSULIN DEPENDENT DIABETES MELLITUS;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
POINT MUTATION;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
RESTRICTION MAPPING;
BASE SEQUENCE;
CASE REPORT;
CELLS, CULTURED;
CHILD;
DEAFNESS;
DIABETES MELLITUS, NON-INSULIN-DEPENDENT;
DNA, MITOCHONDRIAL;
FEMALE;
HELA CELLS;
HETEROZYGOTE DETECTION;
HOMOZYGOTE;
HUMAN;
MALE;
MIDDLE AGE;
MOLECULAR SEQUENCE DATA;
MUSCLES;
OLIGODEOXYRIBONUCLEOTIDES;
PEDIGREE;
POINT MUTATION;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
RESTRICTION MAPPING;
RNA;
RNA, TRANSFER, LEU;
SUPPORT, NON-U.S. GOV'T;
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EID: 0026906885
PISSN: 10614036
EISSN: 15461718
Source Type: Journal
DOI: 10.1038/ng0892-368 Document Type: Article |
Times cited : (1080)
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References (26)
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