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Updated: Feb 7, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Case of late-onset Sandhoff disease due to a novel mutation in the HEXB gene
Angela R Sung1, Paolo Moretti1, Aziz Shaibani1
1Department of Neurology (A.R.S.), Baylor College of Medicine; Neurology Care Line (P.M.), Michael E. DeBakey Veterans Affairs Medical Center; and Nerve and Muscle Center of Texas (A.S.), Houston, TX.
No abstract available in PubMed .
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