Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies.

Human mutation

Volumn 7, Issue 3, 1996, Pages 280-281

  Palmer, M S ^a   van Leeven, R H ^a   Mahal, S P ^a   Campbell, T A ^a   Humphreys, C B ^a   Collinge, J ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

OLIGODEOXYRIBONUCLEOTIDE; RESTRICTION ENDONUCLEASE;

ALLELE; CHEMISTRY; DNA SEQUENCE; EXON; GENETICS; HUMAN; INTRON; LETTER; METABOLISM; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PRION; PRION DISEASE;

ALLELES; BASE SEQUENCE; DNA RESTRICTION ENZYMES; EXONS; HUMANS; INTRONS; MOLECULAR SEQUENCE DATA; MUTATION; OLIGODEOXYRIBONUCLEOTIDES; PRION DISEASES; PRIONS; SEQUENCE ANALYSIS, DNA;

EID: 0029719336     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1996)7:3<280::AID-HUMU17>3.0.CO;2-Z     Document Type: Letter

References (0)