Image of the Month: Locating molecular players in Batten disease
Mutations in either protein CLN6 or CLN8 result in two forms of Batten disease with remarkably similar clinical features. It turns out, as recently shown
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neurodevelopmental disorder
Mouse model helps solve 15q13.3 microdeletion puzzle
Individuals with a complex neurological condition called 15q13.3 microdeletion syndrome are missing a small piece of chromosome 15 that usually contains six genes. Although this
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