Mutations in the Proenteropeptidase Gene Are the Molecular Cause of Congenital Enteropeptidase Deficiency-Reference-Cited by-同舟云学术

Mutations in the Proenteropeptidase Gene Are the Molecular Cause of Congenital Enteropeptidase Deficiency

Published:2002-01 Issue:1 Volume:70 Page:20-25
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Holzinger Andreas,Maier Esther M.,Bück Cornelius,Mayerhofer Peter U.,Kappler Matthias,Haworth James C.,Moroz Stanley P.,Hadorn Hans-Beat,Sadler J. Evan,Roscher Adelbert A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference24 articles.

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2. Distribution of enterokinase activity in the human intestine;Eggermont;Acta Gastroenterol Belg,1971

3. Intestinal enterokinase deficiency;Follett;Acta Paediatr Scand,1976

4. Isolated congenital enterokinase deficiency. Recent findings and review of the literature;Ghishan;Gastroenterology,1983

5. Primary intestinal enteropeptidase deficiency;Green;J Pediatr Gastroenterol Nutr,1984

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