Identification of TSC1 or TSC2 mutation limited to the tumor in three cases of solitary subependymal giant cell astrocytoma using next-generation sequencing technology-Reference-Cited by-同舟云学术

Identification of TSC1 or TSC2 mutation limited to the tumor in three cases of solitary subependymal giant cell astrocytoma using next-generation sequencing technology

Published:2020-02-26 Issue:5 Volume:36 Page:961-965
ISSN:0256-7040
Container-title:Child's Nervous System
language:en
Short-container-title:Childs Nerv Syst

Author:

Fohlen Martine^ORCID,Harzallah Ines,Polivka Marc,Giuliano Fabienne,Pons Linda,Streichenberger Nathalie,Dorfmüller Georg,Touraine Renaud

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00381-020-04551-4.pdf

Reference28 articles.

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2. Chan JA, Zhang H, Roberts PS, Jozwiak S, Wieslawa G, Lewin-Kowalik J et al (2004) Pathogenesis of tuberous sclerosis subependymal giant cell astrocytomas: biallelic inactivation of TSC1 or TSC2 leads to mTOR activation. J Neuropathol Exp Neurol 63:1236–1242

3. (1993) European Chromosome 16 Tuberous Sclerosis Consortium: Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 75:1305–1315

4. Fohlen M, Ferrand-Sorbets S, Delalande O, Dorfmüller G (2018) Surgery for subependymal giant cell astrocytomas in children with tuberous sclerosis complex. Childs Nerv Syst 34:1511–1519

5. Goh S, Butler W, Thiele EA (2004) Subependymal giant cell tumors in tuberous sclerosis complex. Neurology 63:1457–1461

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