Cortical dysplasia associated with the PTEN mutation in Bannayan Riley Ruvalcaba syndrome: a rare finding.
Affiliation
Department of Neurology, Children's University Hospital, Dublin, Ireland. declanorourke@mac.comIssue Date
2012-04MeSH
AdultAmino Acid Substitution
Brain
Exons
Hamartoma Syndrome, Multiple
Humans
Infant
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mutation
PTEN Phosphohydrolase
Metadata
Show full item recordCitation
Cortical dysplasia associated with the PTEN mutation in Bannayan Riley Ruvalcaba syndrome: a rare finding. 2012, 21 (2):91-2 Clin. Dysmorphol.Journal
Clinical dysmorphologyDOI
10.1097/MCD.0b013e328351639dPubMed ID
22327138Item Type
ArticleLanguage
enISSN
1473-5717ae974a485f413a2113503eed53cd6c53
10.1097/MCD.0b013e328351639d
Scopus Count
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