Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN

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Bibliographic Details
Published in:	European journal of pediatrics Vol. 167; no. 6; pp. 671 - 675
Main Authors:	HAUCK, Fabian H, TANNER, Stephan M, HENKER, Jobst, LAASS, Martin W
Format:	Journal Article
Language:	English
Published:	Heidelberg Springer 01-06-2008 Berlin
Subjects:	Biological and medical sciences Gastroenterology. Liver. Pancreas. Abdomen General aspects Medical sciences Nephrology. Urinary tract diseases Other diseases. Semiology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Urinary system involvement in other diseases. Miscellaneous Urinary tract. Prostate gland Europe Germany Human Pediatrics Urinary system disease Megaloblastic anemia Deficiency Funicular myelosis Hemopathy German Compounds Syndrome Heterozygosity Intrinsic factor Intestinal malabsorption Digestive diseases Intestinal disease Female Genetics Cobalamine Intrinsic factor deficiency Mutation Child Megaloblastic anaemia Proteinuria Cobalamin malabsorption
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ISSN:	0340-6199 1432-1076
DOI:	10.1007/s00431-007-0571-3