Literature DB >> 8304353

mtDNA: Pathogenic or nonpathogenic sequence changes.

J Poulton, L A Bindoff.   

Abstract

Mesh：

Substances：

Year:  1994        PMID： 8304353      PMCID： PMC1918168     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  3 in total

1.  Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy.

Authors:  J Poulton; D M Turnbull; A B Mehta; J Wilson; R M Gardiner
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

2.  Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.

Authors:  Y Tatuch; J Christodoulou; A Feigenbaum; J T Clarke; J Wherret; C Smith; N Rudd; R Petrova-Benedict; B H Robinson
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

3.  The clinical features of mitochondrial myopathy.

Authors:  R K Petty; A E Harding; J A Morgan-Hughes
Journal:  Brain       Date:  1986-10       Impact factor: 13.501
  3 in total
  1 in total

1.  Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging.

Authors:  F Pallotti; X Chen; E Bonilla; E A Schon
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.