Glycerol metabolism and the determination of triglycerides - Clinical, biochemical and molecular findings in six subjects

Clinical Chemistry and Laboratory Medicine

Volumn 41, Issue 1, 2003, Pages 46-55

  Hellerud, Christina ^a   Burlina, Alberto ^b   Gabelli, Carlo ^b   Ellis, James R ^c   Nyholm, Per Georg ^d   Lindstedt, Sven ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF PADOVA   (Italy)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

^d UNIVERSITY OF GOTHENBURG   (Sweden)

Author keywords

Congenital adrenal hypoplasia; Glycerol; Glycerol kinase deficiency; Missense mutation; Splice site mutation; Triglycerides

Indexed keywords

CHOLESTEROL; GLYCEROL; GLYCEROL KINASE; MESSENGER RNA; TRIACYLGLYCEROL;

ADRENAL INSUFFICIENCY; ADULT; ANALYTIC METHOD; ARTICLE; CASE REPORT; CHOLESTEROL BLOOD LEVEL; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME DEFICIENCY; ESCHERICHIA COLI; GENE MUTATION; GLYCEROL BLOOD LEVEL; GLYCEROL KINASE DEFICIENCY; HUMAN; HYPERTRIGLYCERIDEMIA; HYPOGLYCEMIA; ITALY; KETOACIDOSIS; MALE; METABOLISM; MISSENSE MUTATION; MOLECULAR MODEL; PRIORITY JOURNAL; SCHOOL CHILD; SYMPTOMATOLOGY; TRIACYLGLYCEROL BLOOD LEVEL;

ADRENAL GLAND DISEASES; ALLELES; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA PRIMERS; DNA-BINDING PROTEINS; FEMALE; GENETIC HETEROGENEITY; GLYCEROL; GLYCEROL KINASE; HUMANS; HYPERTRIGLYCERIDEMIA; MALE; MIDDLE AGED; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; POLYMERASE CHAIN REACTION; RECEPTORS, RETINOIC ACID; REPRESSOR PROTEINS; RNA, MESSENGER; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTORS; TRIGLYCERIDES;

ESCHERICHIA COLI;

EID: 0037216249     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2003.009     Document Type: Article

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