Novel mutations in patients with fructose-1,6-bisphosphatase deficiency

Journal of Inherited Metabolic Disease

Volumn 22, Issue 2, 1999, Pages 132-138

  Herzog, B ^a   Wendel, U ^b   Morris, A A M ^c   Eschrich, K ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b HEINRICH HEINE UNIVERSITY   (Germany)

^c NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FRUCTOSE BISPHOSPHATASE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DNA SEQUENCE; ENZYME DEFICIENCY; EXON; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GLUCONEOGENESIS; HOMOZYGOSITY; HUMAN; INFANT; LEUKOCYTE; MALE; NEWBORN; PRESCHOOL CHILD;

ANIMALS; COS CELLS; FEMALE; FRUCTOSE-BISPHOSPHATASE; HUMANS; INFANT; INFANT, NEWBORN; MALE; METABOLISM, INBORN ERRORS; MUTATION;

EID: 0032924779     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005489617843     Document Type: Article

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