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Article

Analysis of mutations in the SCH gene in schwannomas.

Genes, chromosomes & cancer - 1 Sept 1994

Bijlsma E K, Merel P, Bosch D A, Westerveld A, Delattre O, Thomas G, Hulsebos T J

Abstract excerpt

Schwannomas are benign tumors of cranial, spinal, and other nerve sheaths that develop sporadically or are inherited as part of neurofibromatosis type 2 (NF2). The NF2 gene (SCH) on chromosome 22 has recently been identified and shown to be inactivated by mutation and allele loss in some schwannomas. However, only limited regions in the SCH coding region were examined for mutations. We have extended these studies...

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PMID: 7529050
DOI: 10.1002/gcc.2870110103

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Analysis of mutations in the SCH gene in schwannomas.PMID 7529050Read ↗

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