LIN7A Depletion Disrupts Cerebral Cortex Development, Contributing to Intellectual Disability in 12q21-Deletion Syndrome

Interstitial deletion of 12q21 has been reported in four cases, which share several common clinical features, including intellectual disability (ID), low-set ears, and minor cardiac abnormalities. Comparative genomic hybridization (CGH) analysis using the Agilent Human Genome CGH 180K array was perf...

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Main Authors: Matsumoto, Ayumi, Mizuno, Makoto, Hamada, Nanako, Nozaki, Yasuyuki, Jimbo, Eriko F., Momoi, Mariko Y., Nagata, Koh-ichi, Yamagata, Takanori
פורמט: Artigo
שפה:Inglês
יצא לאור: Public Library of Science 2014
נושאים:
Research Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3962435/
https://ncbi.nlm.nih.gov/pubmed/24658322
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0092695
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