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Updated: Feb 16, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Point mutation in p14ARF -specific exon 1β of CDKN2A causing familial melanoma and astrocytoma
A M McInerney-Leo1, L Wheeler1, R A Sturm2
1Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology (QUT) at Translational Research Institute, Woolloongabba, Queensland, Australia.
No abstract available in PubMed .
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