Work

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

Year: 1999

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/13815

Authors: Sophie Laberge-le Couteulx, Hans H. Jung, Pierre Labauge, Jean-Pierre Houtteville, Christelle Lescoat, Michaelle Cecillon, Emmanuelle Marechal, Anne Joutel, Jean-François Bach, Elisabeth Tournier-Lasserve

Institutions: Inserm, Centre Hospitalier Universitaire de Caen Normandie, Hôpital Lariboisière

Language: English

Topic: Vascular Malformations Diagnosis and Treatment

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1608253138

FWCI: 15.18

Cites: 23

Cited by: 483

Related to: 10