Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene-Reference-Cited by-同舟云学术

Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene

Published:2018-10-16 Issue:4 Volume:129 Page:967-973
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Evans D. Gareth¹^ORCID,Wallace Andrew J.¹,Hartley Claire¹,Freeman Simon R.²,Lloyd Simon K.²,Thomas Owen³,Axon Patrick⁴,Hammerbeck‐Ward Charlotte L.⁵,Pathmanaban Omar⁵,Rutherford Scott A.⁵,Kellett Mark⁶,Laitt Roger³,King Andrew T.⁵,Bischetsrieder Jemma⁷,Blakeley Jaishri⁸,Smith Miriam J.¹

Affiliation:

1. Department of Genomic Medicine Manchester United Kingdom

2. Department of OtolaryngologyUniversity of Manchester, Manchester Academic Health Science Centre, Division of Evolution and Genomic Sciences, Manchester Universities NHS Foundation Trust Manchester United Kingdom

3. Department of NeuroRadiologySalford Royal NHS Foundation Trust Salford Manchester United Kingdom

4. Department of OtolaryngologyAddenbrooke's Hospital Cambridge United Kingdom

5. Department of NeurosurgerySalford Royal NHS Foundation Trust Salford Manchester United Kingdom

6. Department of NeurologySalford Royal NHS Foundation Trust Salford Manchester United Kingdom

7. Department of GeneticsKaiser Permanente Fontana California U.S.A.

8. Johns Hopkins Hospital Baltimore Maryland U.S.A.

Funder

Manchester National Institute for Health Research Biomedical Research Centre

Publisher

Wiley

Subject

Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/lary.27554

Reference16 articles.

1. Multiple synchronous sites of origin of vestibular schwannomas in neurofibromatosis Type 2

2. Incidence of Vestibular Schwannoma and Neurofibromatosis 2 in the North West of England over a 10-year Period: Higher Incidence than Previously Thought

3. A clinical study of type 2 neurofibromatosis;Evans DGR;Q J Med,1992

4. Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1-related schwannomatosis

5. Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young Adults

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