Lyon, Gholson J. (February 2016) New human neurologic and intellectual disability syndromes involving transcription, translation, and protein degradation. In: Columbia Child Neurology and Institute of Genomic Medicine, Columbia University, New York, NY. (Unpublished)
Item Type: | Conference or Workshop Item (Lecture) |
---|---|
Subjects: | bioinformatics diseases & disorders > congenital hereditary genetic diseases bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > transcription bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification diseases & disorders > congenital hereditary genetic diseases > mental retardation bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > translation |
CSHL Authors: | |
Communities: | CSHL labs > Lyon lab |
Depositing User: | Stephanie Hovanec |
Date: | February 2016 |
Date Deposited: | 11 May 2016 16:47 |
Last Modified: | 11 May 2016 16:47 |
URI: | https://repository.cshl.edu/id/eprint/32793 |
Actions (login required)
Administrator's edit/view item |