http://www.cnr.it/ontology/cnr/individuo/prodotto/ID242271
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. (Articolo in rivista)
- Type
- Label
- Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. (Articolo in rivista) (literal)
- Anno
- 1994-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1038/ng1294-323 (literal)
- Alternative label
Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D. (1994)
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy.
in Nature genetics (Print); Nature Publishing Group, London (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.nature.com/ng/journal/v8/n4/abs/ng1294-323.html (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Scopu (literal)
- PubMe (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Genetica Biochimica ed Evoluzionistica CNR, Via Abbiategrasso 207, 27100 Pavia, Italy; Laboratorio di Genetica Molecolare, Istituto G. Gaslini, 16148 Genova, Italy. (literal)
- Titolo
- Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. (literal)
- Abstract
- Emery-Dreifuss muscular dystrophy (EDMD) is an X-linked recessive disorder characterized by slowly progressing contractures, wasting of skeletal muscle and cardiomyopathy. Heart block is a frequent cause of death. The disease gene has been mapped to distal Xq28. Among many genes in this region, we selected eight transcripts expressed at high levels in skeletal muscle, heart and/or brain as the best candidates for the disease. We now report, in all five patients studied, unique mutations in one of the genes, STA: these mutations result in the loss of all or part of the protein. The EDMD gene encodes a novel serine-rich protein termed emerin, which contains a 20 amino acid hydrophobic domain at the C terminus, similar to that described for many membrane proteins of the secretory pathway involved in vesicular transport. (literal)
- Editore
- Prodotto di
- Autore CNR
- Insieme di parole chiave
Incoming links:
- Prodotto
- Autore CNR di
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- Editore di
- Insieme di parole chiave di