Highly Polymorphic Microsatellite Sequences in the Human

Litt, Michael

Abstract

Funding Agency

• Agency: National Institute of Health (NIH)
• Institute: National Human Genome Research Institute (NHGRI)
• Type: Research Project (R01)
• Project #: 5R01HG000022-02
• Application #: 3333040
• Study Section: Special Emphasis Panel (SSS (A))
• Project Start: 1990-06-01
• Project End: 1993-05-31
• Budget Start: 1991-06-01
• Budget End: 1992-05-31
• Support Year: 2
• Fiscal Year: 1991

Institution

• Name: Oregon Health and Science University
• Type: Schools of Medicine
• DUNS #: 009584210
• City: Portland
• State: OR
• Country: United States
• Zip Code: 97239

Publications

Litt, M; Carrero-Valenzuela, R; LaMorticella, D M et al. (1997) Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. Hum Mol Genet 6:665-8

Caryyro-Valenzuela, R; Lindblad, K; Payami, H et al. (1995) No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology 45:1760-3