A thymidine to cytosine substitution for codon 26 of exon 3 of apolipoprotein C-II gene in a patient with apolipoprotein C-II deficiency

Internal Medicine

Volumn 38, Issue 2, 1999, Pages 140-144

  Kuniyoshi, Akiko ^a,c   Okamoto, Yasuyuki ^b   Tamagawa, Taikou ^a   Matsuyama, Yoshinori ^a   Fuku, Hiroshi ^b  

^a Department of Internal Medicine   (Japan)

^b NARA MEDICAL UNIVERSITY   (Japan)

^c Department of Internal Medicine   (Japan)

Author keywords

Chylomicronemia; Mutation; Polymerase chain reaction (PCR); Restriction fragment length polymorphism (RFLP)

Indexed keywords

APOLIPOPROTEIN C; APOLIPOPROTEIN C2; CYTOSINE; DNA; PRIMER DNA; THYMIDINE;

ARTICLE; CASE REPORT; CHEMISTRY; CODON; EXON; FEMALE; GENETICS; HUMAN; HYPERTRIGLYCERIDEMIA; MIDDLE AGED; PANCREATITIS; POINT MUTATION; POLYMERASE CHAIN REACTION; RECURRENT DISEASE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; WESTERN BLOTTING;

APOLIPOPROTEIN C-II; APOLIPOPROTEINS C; BLOTTING, WESTERN; CODON; CYTOSINE; DNA; DNA PRIMERS; EXONS; FEMALE; HUMANS; HYPERTRIGLYCERIDEMIA; MIDDLE AGED; PANCREATITIS; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RECURRENCE; THYMIDINE;

EID: 0033071616     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.38.140     Document Type: Article

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