RT @shanemuk: Here's a gene you've probably never heard of: SPATA5. Mutations are associated with an autosomal recessive syndrome of intell…
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Here's a gene you've probably never heard of: SPATA5. Mutations are associated with an autosomal recessive syndrome of intellectual disability, hearing loss and seizures. We need #genomics to diagnose these #rarediseases https://t.co/aI0VkxClGI
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SPATA5 mutations in a autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss https://t.co/1vfVNn9HMw
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SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hea... https://t.co/e61eXReOqk