Work

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

Year: 2001

Type: article

Study design: Observational Study

Source: Science

DOI: 10.1126/science.1062125

Authors: Christina L. Liquori, Kenneth Ricker, Melinda L. Moseley, Jennifer F. Jacobsen, Wolfram Kress, Susan L. Naylor, John W. Day, Laura P. W. Ranum

Institutions: University of Minnesota, University of Würzburg, The University of Texas at San Antonio Health Science Center

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Human Genome Research Institute, National Cancer Institute, National Institute of Neurological Disorders and Stroke

Awards: CONTINUING MEGABASE SEQUENCING AT THE BCM HGSC, G4515013586, G5738024906, CLONING/CHARACTERIZATING A MYOTONIC DYSTROPHY LOCUS, G7888615315

OpenAlex ID: W1994674028

FWCI: 18.05

Cites: 39

Cited by: 1,223

Related to: 10