Literature DB >> 16266762

Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy.

Golla N Prasad, Ayyasamy Vanniarajan, Cyril Emmanuel, Kotturathu Mammen Cherian, Lalji Singh, Kumarasamy Thangaraj.   

Abstract

We report a rare case of a 65 year old male with mid left ventricular cavity obstruction which is an uncommon form of hypertrophic cardiomyopathy with cytogenetic analysis revealing novel mutations in mitochondrial nucleic acid.

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Year:  2005        PMID： 16266762     DOI： 10.1016/j.ijcard.2005.07.065

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN： 0167-5273            Impact factor:   4.164


  8 in total

1.  Mitochondrial DNA variations in Madras motor neuron disease.

Authors:  Periyasamy Govindaraj; Atchayaram Nalini; Nithin Krishna; Anugula Sharath; Nahid Akhtar Khan; Rakesh Tamang; M Gourie-Devi; Robert H Brown; Kumarasamy Thangaraj
Journal:  Mitochondrion       Date:  2013-02-16       Impact factor: 4.160

2.  Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.

Authors:  Boris Rebolledo-Jaramillo; Marcia Shu-Wei Su; Nicholas Stoler; Jennifer A McElhoe; Benjamin Dickins; Daniel Blankenberg; Thorfinn S Korneliussen; Francesca Chiaromonte; Rasmus Nielsen; Mitchell M Holland; Ian M Paul; Anton Nekrutenko; Kateryna D Makova
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-13       Impact factor: 11.205

3.  Characterization of mtDNA variation in a cohort of South African paediatric patients with mitochondrial disease.

Authors:  Elizna M van der Walt; Izelle Smuts; Robert W Taylor; Joanna L Elson; Douglass M Turnbull; Roan Louw; Francois H van der Westhuizen
Journal:  Eur J Hum Genet       Date:  2012-01-18       Impact factor: 4.246

Review 4.  The Diseased Mitoribosome.

Authors:  Alberto Ferrari; Samuel Del'Olio; Antoni Barrientos
Journal:  FEBS Lett       Date:  2020-12-22       Impact factor: 4.124

Review 5.  Cardiac complications in inherited mitochondrial diseases.

Authors:  Mohaddeseh Behjati; Mohammad Reza Sabri; Masood Etemadi Far; Majid Nejati
Journal:  Heart Fail Rev       Date:  2021-03       Impact factor: 4.214

6.  Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromes.

Authors:  Alberto Gómez-Carballa; María Cerezo; Emilia Balboa; Claudia Heredia; Lidia Castro-Feijóo; Itxaso Rica; Jesús Barreiro; Jesús Eirís; Paloma Cabanas; Isabel Martínez-Soto; Joaquín Fernández-Toral; Manuel Castro-Gago; Manuel Pombo; Ángel Carracedo; Francisco Barros; Antonio Salas
Journal:  PLoS One       Date:  2011-04-19       Impact factor: 3.240

7.  Mitochondriome and cholangiocellular carcinoma.

Authors:  Wesam Bahitham; Xiaoping Liao; Fred Peng; Fiona Bamforth; Alicia Chan; Andrew Mason; Bradley Stone; Paul Stothard; Consolato Sergi
Journal:  PLoS One       Date:  2014-08-19       Impact factor: 3.240

8.  NUMT Confounding Biases Mitochondrial Heteroplasmy Calls in Favor of the Reference Allele.

Authors:  Hannah Maude; Mira Davidson; Natalie Charitakis; Leo Diaz; William H T Bowers; Eva Gradovich; Toby Andrew; Derek Huntley
Journal:  Front Cell Dev Biol       Date:  2019-09-25
  8 in total

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