Related Experiment Video
Updated: Jun 7, 2026

05:51
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Novel TEAD1 Gene Mutation in Sveinsson Chorioretinal Atrophy
Manu Sharma1, Nitin Gautam1, Simar Rajan Singh1
1Advanced Eye Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Ophthalmology. Retina
|June 6, 2026
Summary
No abstract available in PubMed .
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The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
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While point mutations are changes in a single nucleotide in...
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Overview

