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Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome

Acta Neuropathologica

Jan 4, 2020

David SumerauerMichal Zapotocky

Abstract

No abstract listed.

Mentioned in this Paper

IDH1
Li-Fraumeni Syndrome
IDH1 gene
Diffuse Astrocytoma
3
Paper Details
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Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome

Acta Neuropathologica

Jan 4, 2020

David SumerauerMichal Zapotocky

PMID: 31897644

DOI: 10.1007/s00401-019-02118-5

Abstract

No abstract listed.

Mentioned in this Paper

IDH1
Li-Fraumeni Syndrome
IDH1 gene
Diffuse Astrocytoma
3

Similar Papers Found In These Feeds

Li-Fraumeni Syndrome

Li-Fraumeni Syndrome is a rare autosomal dominant syndrome caused by mutations in the tumor suppressor TP53 and characterized by mesenchymal and epithelial neoplasms and several sites. Here is the latest research.

Lysosome & C9orf72

This feed focuses on the C9orf72 protein and its possible role in lysosome function and implication in frontotemporal dementia and amyotrophic lateral sclerosis

Related Papers

Rivista di neurologia

Diffuse astrocytomas

Rivista di neurologiaMarch 1, 1953
A EDERLI, V BRAITENBERG
Journal of the Advanced Practitioner in Oncology

Li-Fraumeni Syndrome

Journal of the Advanced Practitioner in OncologyOctober 19, 2018
Wendy H Vogel
Paper Details
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    References currently unavailable

    We're still populating references for this paper, please check back later.
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