The study of the neurobehavioral consequences of mutations of FMR1, the gene responsible for fragile X syndrome (FraX), has been based largely on correlations between mutation patterns and cognitive profile. Following the characterization of FMRP, the FMR1 gene product, preliminary correlations betw
HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation
✍ Scribed by Karen W. Gripp; Angela E. Lin; Deborah L. Stabley; Linda Nicholson; Charles I. Scott Jr.; Daniel Doyle; Yoko Aoki; Yoichi Matsubara; Elaine H. Zackai; Pablo Lapunzina; Antonio Gonzalez-Meneses; Jennifer Holbrook; Cynthia A. Agresta; Iris L. Gonzalez; Katia Sol-Church
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 104 KB
- Volume
- 140A
- Category
- Article
- ISSN
- 1552-4825
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