Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
Year: 1994
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/3.9.1657
Authors: Dominique Hillaire, Anne Leclerc, Sabine Fauré, Haluk Topaloglu, Nuchanard Chiannllkulchaï, Pascale Guicheney, Laurent Grinas, Patricia Legos, Joanne Philpot, Teresinha Evangelista, Marie-Claude Routon, Michèle Mayer, Jean-Francols Pellissier, Brigitte Estournet, Annie Barols, Fayçal Hentati, Nicole Feingold, Jacqui S.Beckmann, Victor Dubowitz, Fernando M.S.Tomé, Michel Fardeau
Institutions: Genethon (France), Centre National de la Recherche Scientifique, Inserm, Hacettepe University Hospital, Hammersmith Hospital, Hôpital Saint-Vincent-de-Paul, Hôpital de la Timone, Hôpital Raymond-Poincaré, National Institute of Neurology Mongi-Ben Hamida, Château de Longchamp, Fondation Jean Dausset-CEPH
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2167922607