A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes

Clinical Biochemistry

Volumn 32, Issue 2, 1999, Pages 137-141

  Sudo, Kayoko ^a   Maekawa, Masato ^b   Houki, Nobuyuki ^c   Okuda, Takanari ^c   Akizuki, Setsuko ^a   Magara, Tadao ^a   Kawano, Kazuhiro ^d  

^a JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NATIONAL CANCER CENTER HOSPITAL   (Japan)

^c SHIONOGI AND CO LTD   (Japan)

^d Oe Kyoudo Hospital   (Japan)

Author keywords

Expression at mRNA level; Glycolytic pathway; Substrate contact domain; Three dimensional change

Indexed keywords

ASPARAGINE; ISOENZYME; LACTATE DEHYDROGENASE;

ADULT; ARTICLE; CASE REPORT; CONTROLLED STUDY; DNA SEQUENCE; ENZYME ACTIVITY; ENZYME DEFICIENCY; ENZYME SUBUNIT; GENE DELETION; HUMAN; LACTATE DEHYDROGENASE BLOOD LEVEL; MALE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; RESIDUE ANALYSIS;

ADULT; ERYTHROCYTES; HUMANS; ISOENZYMES; L-LACTATE DEHYDROGENASE; MALE; SEQUENCE DELETION;

EID: 0033055248     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-9120(98)00097-6     Document Type: Article

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