Literature DB >> 1978914

Mitochondrial mutation in fatal infantile cardiomyopathy.

M Tanaka, H Ino, K Ohno, K Hattori, W Sato, T Ozawa, T Tanaka, S Itoyama.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1990        PMID： 1978914     DOI： 10.1016/0140-6736(90)93162-i

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  31 in total

1.  Mitochondrial myopathy presenting as ataxia with dilated cardiomyopathy.

Authors:  S Gulati; A Das Gupta; M Kabra; R Juneja; M C Sharma; V Kalra
Journal:  Indian J Pediatr       Date:  2001-04       Impact factor: 1.967

2.  Mitochondrial tRNA(Thr) mutations and lethal infantile mitochondrial myopathy.

Authors:  M D Brown; A Torroni; J M Shoffner; D C Wallace
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

Review 3.  Diseases resulting from mitochondrial DNA point mutations.

Authors:  D C Wallace; M T Lott; J M Shoffner; M D Brown
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy.

Authors:  J Marin-Garcia; R Ananthakrishnan; M J Goldenthal; J J Filiano; A Perez-Atayde
Journal:  J Inherit Metab Dis       Date:  1997-09       Impact factor: 4.982

5.  The mitochondrial A3243G mutation presenting as severe cardiomyopathy.

Authors:  L Vilarinho; F M Santorelli; M J Rosas; C Tavares; M Melo-Pires; S DiMauro
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

6.  A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.

Authors:  K Weber; J N Wilson; L Taylor; E Brierley; M A Johnson; D M Turnbull; L A Bindoff
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

7.  Mitochondrial cardiomyopathy.

Authors:  J Marin-Garcia; M J Goldenthal
Journal:  Pediatr Cardiol       Date:  1995 Jan-Feb       Impact factor: 1.655

8.  Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.

Authors:  J M van den Ouweland; G J Bruining; D Lindhout; J M Wit; B F Veldhuyzen; J A Maassen
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

9.  Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Authors:  D D De Vries; L N Went; G W Bruyn; H R Scholte; R M Hofstra; P A Bolhuis; B A van Oost
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

10.  The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.

Authors:  J Loeffen; J Smeitink; R Triepels; R Smeets; M Schuelke; R Sengers; F Trijbels; B Hamel; R Mullaart; L van den Heuvel
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.