Oligo-astrocytoma in LZTR1-related Noonan syndrome

Oligo-astrocytoma in LZTR1-related Noonan syndrome

Mutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have been recently involved in a small proportion of patients with autosomal dominant and autosomal recessive Noonan syndrome. LZTR1 is also a driver gene in non syndromal glioblastoma. We report a 26-year-old patient...

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Bibliografische gegevens
Hoofdauteurs:	Jacquinet, A, Bonnard, A, Capri, Y, Martin, D, Sadzot, B, Bianchi, E, Servais, L, Sacré, J-P, Cavé, H, Verloes, A
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	Elsevier 2019

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