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Volumn 13, Issue 2, 2009, Pages 167-172
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Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINOACYL TRANSFER RNA;
MITOCHONDRIAL DNA;
RIBOSOME RNA;
RNA, RIBOSOMAL, 12S;
TRNA, SERINE;
TRNA, SERINE-;
ADOLESCENT;
ADULT;
AGED;
ARTICLE;
CAUCASIAN;
CHILD;
COHORT ANALYSIS;
ETHNIC AND RACIAL GROUPS;
FEMALE;
GENE DELETION;
GENETIC POLYMORPHISM;
GENETIC SCREENING;
GENETICS;
GEOGRAPHY;
HEARING IMPAIRMENT;
HETEROZYGOTE;
HUMAN;
MALE;
METHODOLOGY;
MIDDLE AGED;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
POLAND;
PRESCHOOL CHILD;
SEQUENCE ANALYSIS;
SINGLE STRAND CONFORMATION POLYMORPHISM;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
COHORT STUDIES;
DEAFNESS;
DNA MUTATIONAL ANALYSIS;
DNA, MITOCHONDRIAL;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
FEMALE;
GENE DELETION;
GENETIC SCREENING;
GEOGRAPHY;
HETEROZYGOTE;
HUMANS;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION;
POLAND;
POLYMORPHISM, GENETIC;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
POPULATION GROUPS;
RNA, RIBOSOMAL;
RNA, TRANSFER, AMINO ACYL;
SEQUENCE ANALYSIS, RNA;
YOUNG ADULT;
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EID: 67650073390
PISSN: None
EISSN: 19450257
Source Type: Journal
DOI: 10.1089/gtmb.2008.0098 Document Type: Article |
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Times cited : (34)
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References (0)
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