Hereditary deficiency of lactate dehydrogenase H-subunit

Internal Medicine

Volumn 35, Issue 7, 1996, Pages 550-554

  Wakabayashi, Hajime ^a,c   Tsuchiya, Masao ^a   Yoshino, Ken ^a   Kaku, Kohei ^b   Shigei, Hiroshi ^a  

^a Shigei Hospital   (Japan)

^b YAMAGUCHI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c OKAYAMA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

Autosomal recessive inheritance; Complete deficiency; Dihydroxyacetonephosphate; Fructose 1,6 diphosphate; Glyceraldehyde 3 phosphate; Hemolysis

Indexed keywords

DIHYDROXYACETONE PHOSPHATE; FRUCTOSE 1,6 BISPHOSPHATE; FRUCTOSE BISPHOSPHATE; FRUCTOSE-1,6-DIPHOSPHATE; GLYCERALDEHYDE 3 PHOSPHATE; ISOENZYME; LACTATE DEHYDROGENASE;

ARTICLE; BLOOD; CASE REPORT; CHEMISTRY; CONSANGUINITY; DIABETES MELLITUS; ENZYMOLOGY; ERYTHROCYTE; FEMALE; GENETICS; GLYCOLYSIS; HEMOLYSIS; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MALE; MIDDLE AGED; PEDIGREE; PROTEIN CONFORMATION; RECESSIVE GENE;

CONSANGUINITY; DIABETES MELLITUS; DIHYDROXYACETONE PHOSPHATE; ERYTHROCYTES; FEMALE; FRUCTOSEDIPHOSPHATES; GENES, RECESSIVE; GLYCERALDEHYDE 3-PHOSPHATE; GLYCOLYSIS; HEMOLYSIS; HETEROZYGOTE; HOMOZYGOTE; HUMANS; ISOENZYMES; L-LACTATE DEHYDROGENASE; MALE; MIDDLE AGED; PEDIGREE; PROTEIN CONFORMATION;

EID: 0030179986     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.35.550     Document Type: Article

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