SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): Genotype/phenotype correlations with disease severity
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference29 articles.
1. A Multicopy Dinucleotide Marker That Maps Close to the Spinal Muscular Atrophy Gene
2. Structure and Organization of the Human Survival Motor Neurone (SMN) Gene
3. A frame–shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients
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