A Roadmap to Newborn Screening for Duchenne Muscular Dystrophy
Author:
Publisher
MDPI AG
Subject
Obstetrics and Gynaecology,Immunology and Microbiology (miscellaneous),Pediatrics, Perinatology, and Child Health
Link
http://www.mdpi.com/2409-515X/3/2/8/pdf
Reference38 articles.
1. Evidence-based path to newborn screening for duchenne muscular dystrophy
2. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
3. The rate of spontaneous mutation of a human gene
4. Risk assessment and genetic counseling in families with Duchenne muscular dystrophy;Grimm;Acta Myol.,2012
5. Clinical and genetic characterization of manifesting carriers of DMD mutations
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1. Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy;Journal of Neuromuscular Diseases;2023-01-03
2. Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot;International Journal of Neonatal Screening;2022-09-22
3. Duchenne expert physician perspectives on Duchenne newborn screening and early Duchenne care;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-06
4. Disease Progression Stages and Burden in Patients with Duchenne Muscular Dystrophy Using Administrative Claims Supplemented by Electronic Medical Records;Advances in Therapy;2022-04-23
5. Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000‐2015;Muscle & Nerve;2022-04-11
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