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Volumn 7, Issue 4, 1996, Pages 379-380
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Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
PRIMER DNA;
TYROSINE;
BLOOD;
DISORDERS OF AMINO ACID AND PROTEIN METABOLISM;
ETHNOLOGY;
FINLAND;
GENETICS;
HETEROZYGOTE;
HETEROZYGOTE DETECTION;
HUMAN;
LETTER;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
AMINO ACID METABOLISM, INBORN ERRORS;
BASE SEQUENCE;
DNA PRIMERS;
FINLAND;
HETEROZYGOTE;
HETEROZYGOTE DETECTION;
HUMANS;
MOLECULAR SEQUENCE DATA;
MUTATION;
TYROSINE;
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EID: 0029704286
PISSN: 10597794
EISSN: None
Source Type: Journal
DOI: 10.1002/(sici)1098-1004(1996)7:4<379::aid-humu20>3.0.co;2-z Document Type: Letter |
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Times cited : (5)
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References (0)
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