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Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)
Hayashi S,
Uehara DT,
Tanimoto K,
Mizuno S,
Chinen Y,
et al.
(2017)
Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH).
PLOS ONE 12(8): e0181791.
https://doi.org/10.1371/journal.pone.0181791