Literature DB >> 11437868

Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family.

L Rigoli, F Prisco, R A Caruso, D Iafusco, G Ursomanno, D Zuccarello, N Ingenito, M Rigoli, I Barberi.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2001        PMID： 11437868     DOI： 10.1046/j.1464-5491.2001.00429-2.x

Source DB:  PubMed          Journal:  Diabet Med        ISSN： 0742-3071            Impact factor:   4.359


× No keyword cloud information.
  3 in total

Review 1.  Mitochondrial diabetes mellitus.

Authors:  J A Maassen; G M C Janssen; H H J P Lemkes
Journal:  J Endocrinol Invest       Date:  2002-05       Impact factor: 4.256

2.  Deepening the knowledge of rare diseases dependent on angiogenesis through semantic similarity clustering and network analysis.

Authors:  Raquel Pagano-Márquez; José Córdoba-Caballero; Beatriz Martínez-Poveda; Ana R Quesada; Elena Rojano; Pedro Seoane; Juan A G Ranea; Miguel Ángel Medina
Journal:  Brief Bioinform       Date:  2022-07-18       Impact factor: 13.994

3.  Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene.

Authors:  Johan L K Van Hove; Cynthia Freehauf; Shelley Miyamoto; Georgirene D Vladutiu; Jacklyn Pancrudo; Eduardo Bonilla; Mark A Lovell; Gary W Mierau; Janet A Thomas; Sara Shanske
Journal:  Eur J Pediatr       Date:  2007-09-22       Impact factor: 3.183
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.