Literature DB >> 961414

Intestinal enterokinase deficiency.

G F Follett, T H Macdonald.   

Abstract

Deficiency of intestinal enterokinase results in failure to thrive, diarrhoea, anaemia, hypoproteinaemia and oedema. A case arising in the neonatal period is described, in which several of the characteristic features were lacking. Difficulties encountered in the diagnosis and methods of assay are discussed.

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Year:  1976        PMID： 961414     DOI： 10.1111/j.1651-2227.1976.tb04948.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


  2 in total

1.  Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.

Authors:  Andreas Holzinger; Esther M Maier; Cornelius Bück; Peter U Mayerhofer; Matthias Kappler; James C Haworth; Stanley P Moroz; Hans-Beat Hadorn; J Evan Sadler; Adelbert A Roscher
Journal:  Am J Hum Genet       Date:  2001-11-21       Impact factor: 11.025

2.  Enteropeptidase: a gene associated with a starvation human phenotype and a novel target for obesity treatment.

Authors:  Sandrine Braud; Marco A Ciufolini; Itzik Harosh
Journal:  PLoS One       Date:  2012-11-21       Impact factor: 3.240
  2 in total

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