Work

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1

Year: 2000

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/9.2.237

Authors: E. Ars, E Serra, J García, H Kruyer, A Gaona, C Lázaro, X Estivill

Institution: Duran i Reynals Hospital

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

OpenAlex ID: W2111090400

FWCI: 13.77

Cites: 57

Cited by: 368

Related to: 10