Newborn and carrier screening for spinal muscular atrophy. [electronic resource]
- American journal of medical genetics. Part A Jul 2010
- 1608-16 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1552-4833
10.1002/ajmg.a.33474 doi
Fluorescence Genotype Health Surveys Heterozygote Humans Infant, Newborn Muscular Atrophy, Spinal--diagnosis Neonatal Screening Survival of Motor Neuron 1 Protein--genetics