Mbnl2 loss alters novel context processing and impairs object recognition memory

Author:

Khandelwal Abinash,Cushman Jesse,Choi Jongkyu,Zhuravka Irina,Rajbhandari Abha,Valiulahi Parvin,Li Xiandu,Zhou Chenyu,Comai Lucio,Reddy Sita

Funder

NIH

University of California, Los Angeles

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference74 articles.

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3. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member;Brook;Cell,1992

4. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy;Harley;Am. J. Hum. Genet.,1993

5. Brain disease and molecular analysis in myotonic dystrophy;Damian;Neuroreport,1994

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