221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

Author:

Bentler Kristi,Zhai Shaohui,Elsbecker Sara A.,Arnold Georgianne L.,Burton Barbara K.,Vockley Jerry,Cameron Cynthia A.,Hiner Sally J.,Edick Mathew J.,Berry Susan A.ORCID,Thomas Janet,Dodge Melinda,Singh Rani,Lakshman Sangeetha,Coakley Katie,Stembridge Adrya,Russi Alvaro Serrano,Phillips Emily,Burton Barbara,Edano Clare,Shrestha Sheela,Hoganson George,Dwyer Lauren,Hainline Bryan,Romie Susan,Hainline Sarah,Asamoah Alexander,Goodin Kara,Rajakaruna Cecilia,Jackson Kelly,Hamosh Ada,Vernon Hilary,Smith Nancy,Ahmad Ayesha,Lipinski Sue,Feldman Gerald,Berry Susan,Elsbecker Sara,Bentler Kristi,Font-Montgomery Esperanza,Peck Dawn,Pena Loren D.M.,Koeberl Dwight D.,Jiang Yong-hui,Kishnani Priya S.,Rizzo William,Dawson Machelle,Ambrose Nancy,Levy Paul,Kronn David,Fong Chin-to,D’Aco Kristin,Hart Theresa,Erbe Richard,Samons Melissa,Leslie Nancy,Powers Racheal,Bartholomew Dennis,Goff Melanie,vanCalcar Sandy,Hansen Joyanna,Arnold Georgianne,Vockley Jerry,Walsh-Vockley Cate,Rhead William,Dimmock David,Engelking Paula,Bird Cassie,Swan Ashley,Schwoerer Jessica Scott,Henry Sonja,Narumanchi TaraChandra,Hummel Marybeth,Wilkins Jennie,Davis-Keppen Laura,Stein Quinn,Loman Rebecca,Cameron Cynthia,Edick Mathew J.,Hiner Sally J.,Justice Kaitlin,Zhai Shaohui

Funder

Eunice Kennedy Shriver National Institute of Child Health and Development (NICHD), National Institutes of Health

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference40 articles.

1. Birth prevalence of disorders detectable through newborn screening by race/ethnicity;Feuchtbaum;Genet. Med.,2012

2. Medium-chain acyl-coenzyme A dehydrogenase deficiency;Matern,2000

3. Outcome of medium chain acyl-CoA dehydrogenase defciency after diagnosis;Wilson;Arch. Dis. Child.,1999

4. MCAD deficiency in Denmark;Andresen;Mol. Genet. Metab.,2012

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