OpenAlex
PricingAboutJobs
Log inGet started
Work

Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13

HTML

Year: 2003
Type: article
Study design: Observational Study
Source: Human Genetics
DOI: 10.1007/s00439-003-0967-8
Authors: Lisbeth Tranebjaerg, Tanya M. Teslovich, MaryPat Jones, M. Michael Barmada, Toril Fagerheim, Arve Dahl, Diana M. Escolar, Jeffrey M. Trent, Elizabeth M. Gillanders, Dietrich A. Stephan
Institutions: University of Copenhagen, Bispebjerg Hospital, National Institutes of Health, Children's National, National Human Genome Research Institute, University of Pittsburgh, University Hospital of North Norway, Oslo University Hospital, Translational Genomics Research Institute
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

Funder: Eunice Kennedy Shriver National Institute of Child Health and Human Development
Award: G1524969718
OpenAlex ID: W2065980971
FWCI: 0.335
Cites: 3
Cited by: 30
Related to: 10
OpenAlex
Nonprofit
Open DataOpen Data
Open Source
Product
Search
Compare
Pricing
Repositories
Unpaywall
Unsub
Developers
API docs
Data snapshot
Status
Source code
Organization
About
Team
Testimonials
Brand
Jobs
Community
Help center
Contact
Events
Blog
Mailing list
Supporters
Legal
Privacy
Accessibility
Terms