Work

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels ofFMR1 messenger RNA

Year: 2000

Type: article

Study design: Observational Study

Source: American Journal of Medical Genetics

DOI: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h

Authors: Flora Tassone, Randi J. Hagerman, Danuta Z. Loesch, Ave Lachiewicz, Annette K. Taylor, Paul J. Hagerman

Institutions: University of Colorado Health, University of Colorado Anschutz, University of Colorado Denver, La Trobe University, Duke Medical Center

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: closed

Funders: National Institutes of Health, National Institute of General Medical Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1500619533, G305629206, PROTEIN NUCLEIC ACID INTERACTIONS, Genotype-Phenotype Relationships in Fragile X Families

OpenAlex ID: W2034014202

FWCI: 3.893

Cites: 33

Cited by: 143

Related to: 10