Müller-Felber, Wolfgang <br/><br/>
Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening - Opportunity or Burden?  [electronic resource] 

 -  Journal of neuromuscular diseases  2020 
 - 109-117 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2214-3602 
<br/><br/><label>Standard No.: </label>10.3233/JND-200475  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Follow-Up Studies<br/>Germany<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Muscular Atrophy, Spinal--diagnosis<br/>Neonatal Screening<br/>Pedigree<br/>Pilot Projects<br/>Survival of Motor Neuron 1 Protein--genetics<br/>Survival of Motor Neuron 2 Protein--genetics