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Updated: May 13, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Published on: June 15, 2011

Spinal muscular atrophy due to a "de novo" 1.3 Mb deletion: implication for genetic counseling

Luciana Rodrigues Jacy da Silva1, Mileny Esbravatti Stephano Colovati, Bruno Coprerski

  • 1Medical Genetics Center, Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.

Neuromuscular Disorders : NMD
|March 5, 2013
PubMed

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