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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease astrocytoma
Comorbidity C0079419|li-fraumeni syndrome
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PubMedID- 20714900 Interestingly, all five examined astrocytomas of patients with li-fraumeni syndrome carried r132c idh1 mutations, indicating that glial/glioma precursor cells with a germline tp53 mutation carry an increased risk to acquire such a non-r132h mutation [130].

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