Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
New York State Office for People With Developmental Disabilities · Tufts University · +7 more institutions
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Abstract
No abstract available for this paper.
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2,199
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Authors
17- MEMaria ErikssonCorresponding
New York State Office for People With Developmental Disabilities
- WTW. Ted Brown
New York State Office for People With Developmental Disabilities
- LBLeslie B. Gordon
Tufts University, Providence College, Rhode Island Hospital
- MWMichael W. Glynn
National Institutes of Health, National Human Genome Research Institute
- JIJoel I. Singer
University of Michigan–Ann Arbor
Topics & keywords
Keywords
- Progeria
- LMNA
- Lamin
- Biology
- Genetics
- Exon
- Point mutation
- Premature aging
UN Sustainable Development Goals
- Good health and well-being
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