Co-occurrence of the Poland sequence in a patient with the cobalamin C defect: more than just a coincidence?

Saved in:

Bibliographic Details
Published in:	Journal of inherited metabolic disease Vol. 38; no. 2; pp. 365 - 366
Main Authors:	Weisfeld-Adams, James D., Baker, Peter R.
Format:	Journal Article
Language:	English
Published:	Dordrecht Springer Netherlands 01-03-2015 Blackwell Publishing Ltd
Subjects:	Biochemistry Carrier Proteins - genetics Genetic Predisposition to Disease Homocystinuria - diagnosis Homocystinuria - genetics Human Genetics Humans Images in Metabolic Medicine Infant, Newborn Internal Medicine Male Medicine Medicine & Public Health Metabolic Diseases Pediatrics Phenotype Poland Syndrome - diagnosis Poland Syndrome - genetics Sequence Deletion Vitamin B 12 Deficiency - congenital Vitamin B 12 Deficiency - diagnosis Vitamin B 12 Deficiency - genetics Cobalamin Methylmalonic Hyperhomocysteinemia Homocysteine Newborn Screening
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Bibliography:	Communicated by: Carlo Dionisi‐Vici ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3
ISSN:	0141-8955 1573-2665
DOI:	10.1007/s10545-014-9791-7