Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

Journal of Pediatrics

Volumn 131, Issue 5, 1997, Pages 766-768

  Tyni, T ^a   Rapola, J ^a   Palotie, A ^a   Pihko, H ^a  

^a UNIVERSITY OF HELSINKI AND HELSINKI UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; LONG CHAIN FATTY ACID; MITOCHONDRIAL ENZYME; PARATHYROID HORMONE;

ARTICLE; CARDIOMYOPATHY; CASE REPORT; ENZYME DEFICIENCY; FATTY ACID OXIDATION; GENE MUTATION; HUMAN; HYPERPHOSPHATEMIA; HYPOCALCEMIA; HYPOGLYCEMIA; HYPOPARATHYROIDISM; INFANT; LIVER DISEASE; MALE; MUSCLE HYPOTONIA; PRIORITY JOURNAL; RETINOPATHY;

EID: 0030816840     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)70111-2     Document Type: Article

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