Molecular genetic analysis in a case of ganglioglioma: Identification of a new mutation

Neurosurgery

Volumn 63, Issue 5, 2008, Pages 976-980

  De Tommasi, Antonio ^a   Luzzi, Sabino ^a   D'Urso, Pietro I ^a   De Tommasi, Claudio ^a   Resta, Nicoletta ^a   Ciappetta, Pasqualino ^a  

^a UNIVERSITY OF BARI   (Italy)

Author keywords

Cerebral ganglioma; Peutz Jeghers syndrome; STK11 LKB1

Indexed keywords

NUCLEOTIDE;

ADULT; ARTICLE; BLOOD; CASE REPORT; EXON; FEMALE; GENE DELETION; GENE INSERTION; GENE MUTATION; GLIOMA; GLIOMA CELL; HUMAN; MOLECULAR GENETICS; PEUTZ JEGHERS SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA ANALYSIS; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

BRAIN NEOPLASMS; CALCINOSIS; FEMALE; FRAMESHIFT MUTATION; FRONTAL LOBE; GANGLIOGLIOMA; HUMANS; PEUTZ-JEGHERS SYNDROME; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN-SERINE-THREONINE KINASES; TOMOGRAPHY, X-RAY COMPUTED;

EID: 57649118659     PISSN: 0148396X     EISSN: None     Source Type: Journal    
DOI: 10.1227/01.NEU.0000327699.93146.CD     Document Type: Article

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