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XLMRX-Linked Mental Retardation
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Fragile X syndrome (FRAXA) (MIM 309550) is the most common cause of monogenic X-linked mental retardation (XLMR) with a worldwide prevalence of nearly 1 in 4000 males and 1 in 8000 females (1).
The purpose of this research then is to explore GPR50, a gene located in chromosomal region Xq28, for its possible involvement in X-Linked Mental Retardation (XLMR).
Hagerman, Seaside Therapeutics (immediate family member), Roche (immediate family member), Novartis (immediate family member), New Orleans Human Development Center Institute, Movement Disorder Society 12th International Congress, Colorado Clinical Scholars Seminar, Nanomedicine Workshop, Nanomedicine Retreat, Washington University Brain Awareness Week, XLMR Meeting (Brazil), and University of California San Francisco Memory and Aging Center.