FOXG1 studies

Reference: Angus Clarke Abstract: Under the supervision of Professor Angus Clarke, Dr David Millar will continue research of the identification of mutations in the FOXG1 gene, This project will work with the E-Rare project in Europe. PROJECT DETAILS  beginning: 2012. end: 2013. Country of research: United Kingdom Counry of funding source: United Kingdom Funding organization: … Read more

Cell line and DNA bank of Rett syndrome and other x-linked mental retardation

Reference: GTF02006 Abstract: Mental retardation (MR) is the most frequent cause of serious handicap in humans with an estimated total prevalence of 1-1,5% in the general population. It is calculated that X-linked MR (XLMR) may account for about 20-25% of mentally retarded males. Up to now, 42 genes have been found involved in XLMR, comprising … Read more

Cell lines and DNA bank of Rett syndrome and other X-linked mental retardation

Reference: GTF05005 Abstract: Mental retardation (MR) is the most frequent cause of serious handicap in humans and an important health-care problem throughout the world. It is estimated to occur in about 1-3% of the general population. It is calculated that X-linked mental retardation (XLMR) may account for about 20ヨ25% of mentally retarded males. The number … Read more

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