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Brown-Vialetto-Van Laere Syndrome 1
A Brown-Vialetto-Van Laere syndrome that is characterized by progressive bulbar palsy with sensorineural deafness that is caused by homozygous or compound heterozygous mutation in the C20ORF54 gene (SLC52A3) on chromosom
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Overview
A Brown-Vialetto-Van Laere syndrome that is characterized by progressive bulbar palsy with sensorineural deafness that is caused by homozygous or compound heterozygous mutation in the C20ORF54 gene (SLC52A3) on chromosom
Resources
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