Hereditary ceroid-lipofuscinosis in English setters has been proposed to be the canine equivalent of human juvenile ceroid-lipofuscinosis, which results from defects in the CLN3 gene. Analyses were performed to determine whether the disease in English setters is also the consequence of a CLN3 gene m
Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder
✍ Scribed by Vourc'h, Patrick ;Petit, Elisabeth ;Müh, Jean Pierre ;Andres, Christian ;Bienvenu, Thierry ;Beldjord, Cherif ;Chelly, Jamel ;Barthélémy, Catherine
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 53 KB
- Volume
- 108
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The gene for the gastrin-releasing peptide receptor (GRPR) has been mapped to a candidate region for Rett syndrome (RTT) on the short arm of the X chromosome. The recent report of a translocation that disrupted the gene in an individual with mental retardation and autistic behavior prompted us to ex
A DEAD box gene (DDXI) characterized by a motif with a putative RNA helicase was found at elevated levels, with multiple copies, in a neuroblastorna and in some retinoblastoma cell lines in which the MYCN gene was amplified. The present study was aimed at determining whether amplification o f the DD
Genes involved in estrogen pathways have been proposed as possible candidates influencing susceptibility to bipolar disorder and the affective symptoms suffered by many women during the puerperal period. The estrogen receptor alpha (ERalpha) gene in particular has been a subject of interest and has