Literature DB >> 10604149

Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation.

M A Martín1, Y Campos, M T García-Silva, J C Rubio, P Del Hoyo, F de Bustos, A García, J Arenas.   

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Year:  1999        PMID： 10604149     DOI： 10.1023/a:1005603926730

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  6 in total

1.  Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

Authors:  J P Jenuth; A C Peterson; K Fu; E A Shoubridge
Journal:  Nat Genet       Date:  1996-10       Impact factor: 38.330

2.  A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Authors:  I J Holt; A E Harding; R K Petty; J A Morgan-Hughes
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

Review 3.  Mitochondrial genetics '98 is the bottleneck cracked?

Authors:  J Poulton; V Macaulay; D R Marchington
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

Review 4.  Bottlenecks and beyond: mitochondrial DNA segregation in health and disease.

Authors:  G K Brown
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

5.  Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes.

Authors:  R B Blok; D A Gook; D R Thorburn; H H Dahl
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

6.  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
  6 in total

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