Work

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

Year: 2008

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2008.01060.x

Authors: C Boyd, MJ Smith, L Kluwe, A Balogh, M MacCollin, SR Plotkin

Institutions: Massachusetts General Hospital, University Medical Center Hamburg-Eppendorf, Center for Neuro-Oncology

Language: English

Topic: Neurofibromatosis and Schwannoma Cases

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institute of Neurological Disorders and Stroke

Award: Molecular Genetics of Inherited Neurological Diseases

OpenAlex ID: W1999340868

FWCI: 10.41

Cites: 38

Cited by: 155

Related to: 10