Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum. uri icon

Overview

publication date

  • March 25, 2014

Research

keywords

  • Genome
  • Malformations of Cortical Development
  • Microcephaly
  • Occludin
  • Polymicrogyria

Identity

Scopus Document Identifier

  • 84899907222

Digital Object Identifier (DOI)

  • 10.1002/ajmg.a.36485

PubMed ID

  • 24668585

Additional Document Info

volume

  • 164A

issue

  • 6