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The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo

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Year: 2005
Type: article
Source: Neurobiology of Disease
DOI: 10.1016/j.nbd.2005.08.019
Authors: E.J. Mientjes, I. Nieuwenhuizen, L. Kirkpatrick, T. Zu, M. Hoogeveen-Westerveld, L. Severijnen, M. Rifé, R. Willemsen, D.L. Nelson, B.A. Oostra
Institutions: Erasmus MC, Erasmus University Rotterdam, Baylor College of Medicine, University of Minnesota
Language: English

Topic: Genetics and Neurodevelopmental Disorders
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1179207774, MOLECULAR ANALYSIS OF FRAGILE X SYNDROME, G534466378, Baylor Intellectual and Developmental Disabilities Research Center, G567197870, Fragile X Related Genes Mental Retardation/Development
OpenAlex ID: W2024955503
FWCI: 1.008
Cites: 33
Cited by: 285
Related to: 10
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