Genotypic differences of MCAD deficiency in the Asian population: Novel genotype and clinical symptoms preceding newborn screening notification-Reference-Cited by-同舟云学术

Genotypic differences of MCAD deficiency in the Asian population: Novel genotype and clinical symptoms preceding newborn screening notification

Published:2005-05 Issue:5 Volume:7 Page:339-343
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Ensenauer Regina,Winters Jennifer L.,Parton Patricia A.,Kronn David F.,Kim Jong-Won,Matern Dietrich,Rinaldo Piero,Hahn Si Houn

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference21 articles.

1. Matern D, Rinaldo P. Medium-chain acyl-coenzyme A dehydrogenase deficiency. In: GeneReviews: Genetic Disease Online Reviews at GeneTests-GeneClinics [database online: Initial posting: April 20, 2000; last update January 27, 2003]. University of Washington, Seattle. Available at: http://www.geneclinics.org Accessed January 2, 2005.

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