Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas

BackgroundMultiple meningiomas occur in

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of medical genetics 2011-02, Vol.48 (2), p.93-97
Hauptverfasser:	Christiaans, I, Kenter, S B, Brink, H C, van Os, T A M, Baas, F, van den Munckhof, P, Kidd, A M J, Hulsebos, T J M
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Base Sequence Biological and medical sciences Cardiovascular disease Chromosomal Proteins, Non-Histone - genetics DNA Mutational Analysis DNA Primers - genetics DNA-Binding Proteins - genetics Epilepsy Female Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genes, Neurofibromatosis 2 Genetics of eukaryotes. Biological and molecular evolution Genotype Germ-Line Mutation - genetics Humans Male Medical genetics Medical sciences Meningioma - genetics Meningioma - pathology Microsatellite Repeats - genetics Molecular and cellular biology Molecular genetics Molecular Sequence Data Mutation Mutation, Missense - genetics neuro oncology Neurology Patients Pedigree SMARCB1 Protein Spinal cord Surgery Transcription Factors - genetics Tumors Tumors of the nervous system. Phacomatoses Twins
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Beschreibung
Zusammenfassung:	BackgroundMultiple meningiomas occur in
ISSN:	0022-2593 1468-6244 1468-6244
DOI:	10.1136/jmg.2010.082420