Severe white matter damage in SHANK3 deficiency: a human and translational study
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DOI: 10.1002/acn3.50959
Abstract: Heterozygous SHANK3 mutations or partial deletions of the long arm of chromosome 22, also known as Phelan–McDermid syndrome, result in a syndromic form of the autism spectrum as well as in global developmental delay, intellectual… read more here.
Keywords: deficiency human; shank3 deficiency; severe white; matter damage ... See more keywords