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See Latest ArticlesSkeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
Human Molecular Genetics, 11/25/09
Clark AR et al. – The data provide the first biochemical evidence for a gain–of–function mechanism for the OPD disorders, and mechanistically distinguishes them from the loss–of–function phenotypes that manifest as disorders of neuronal migration.
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Today in Basic Science/Genetics...keeping you current
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HO-1 polymorphism as a genetic determinant behind the malaria resistance afforded by haemolytic disorders
Medical Hypotheses, 02/09/10
Potocki-Shaffer syndrome: Comprehensive clinical assessment, review of the literature, and proposals for medical management
American Journal of Medical Genetics, 02/09/10
FOXE3 plays a significant role in autosomal recessive microphthalmia
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Today in Neurology...keeping you current
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New frontiers of cognitive rehabilitation in geriatric age: the Mozart Effect (ME)
Archives of Gerontology and Geriatrics, 02/09/10
Capsaicin jelly against migraine pain
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