A case of new PCDH12 gene variants presented as dyskinetic cerebral palsy with epilepsy

Epigenetic dysregulation of protocadherins in human disease

(2017) Nady El Hajj et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders

(2016) Yu Kobayashi et al.   BRAIN & DEVELOPMENT

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection

(2016) Adi Aran et al.   NEUROLOGY

Emerging roles of protocadherins: from self-avoidance to enhancement of motility

(2015) S. Hayashi et al.   JOURNAL OF CELL SCIENCE

Protocadherin-12 Cleavage Is a Regulated Process Mediated by ADAM10 Protein

(2011) Stéphanie Bouillot et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Non-clustered protocadherin

(2011) Soo-Young Kim et al.   Cell Adhesion & Migration

Lesions in the central tegmental tract in autopsy cases of developmental brain disorders

(2010) Mutsuki Shioda et al.   BRAIN & DEVELOPMENT

Symmetrical central tegmental tract (CTT) hyperintense lesions on magnetic resonance imaging in children

(2008) Shoko Yoshida et al.   EUROPEAN RADIOLOGY

Protocadherin 12 deficiency alters morphogenesis and transcriptional profile of the placenta

(2008) Christine Rampon et al.   PHYSIOLOGICAL GENOMICS