Work

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)

Year: 2008

Type: article

Study design: Observational Study

Source: Cytogenetics and Cell Genetics

DOI: 10.1159/000133643

Authors: E. Le Guern, F. Sturtz, M. Gugenheim, R. Gouider, C. Bonnebouche, N. Ravisé, P.-M. Gonnaud, S. Tardieu, P. Bouche, G. Chazot, Y. Agid, A. Vandenberghe, A. Brice

Institutions: Inserm, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements, Hôpital de l'Antiquaille, Lyon 1 Université

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Javna Agencija za Raziskovalno Dejavnost RS

OpenAlex ID: W2084756226

FWCI: 0.577

Cites:

Cited by: 48

Related to: 10