Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Estefania Piñero"'
Autor:
Damian Heine-Suñer, Konstantin Strauch, Clemens Baumbach, Jordi Rosell, Fernando García Algas, Pablo García-Pavía, Luis Alonso-Pulpón, María Angeles de la Fuente Sanchez, Antònia Flaquer, Jorge Toquero, Estefania Piñero
Publikováno v:
BMC Genet. 14:44 (2013)
BMC Genetics
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
BMC Genetics
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Background: Congenital heart defects (CHD) is the most common cause of death from a congenital structure abnormality in newborns and is often associated with fetal loss. There are many types of CHD. Human genetic studies have identified genes that ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::295c683dbae0de7a6a4fd277bdef22f5
https://doi.org/10.1186/1471-2156-14-44
https://doi.org/10.1186/1471-2156-14-44
Autor:
Emmanuelle C Genin, Morgane Plutino, Sylvie Bannwarth, Elodie Villa, Eugenia Cisneros‐Barroso, Madhuparna Roy, Bernardo Ortega‐Vila, Konstantina Fragaki, Françoise Lespinasse, Estefania Pinero‐Martos, Gaëlle Augé, David Moore, Florence Burté, Sandra Lacas‐Gervais, Yusuke Kageyama, Kie Itoh, Patrick Yu‐Wai‐Man, Hiromi Sesaki, Jean‐Ehrland Ricci, Cristofol Vives‐Bauza, Véronique Paquis‐Flucklinger
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 1, Pp 58-72 (2015)
Abstract CHCHD10‐related diseases include mitochondrial DNA instability disorder, frontotemporal dementia‐amyotrophic lateral sclerosis (FTD‐ALS) clinical spectrum, late‐onset spinal motor neuropathy (SMAJ), and Charcot–Marie–Tooth diseas
Externí odkaz:
https://doaj.org/article/a6eda45384124c2da28b788438fcf63d
