41 related articles for article (PubMed ID: 9412783)
1. mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
Lamminen T; Huoponen K; Sistonen P; Juvonen V; Lahermo P; Aula P; Nikoskelainen E; Savontaus ML
Eur J Hum Genet; 1997; 5(5):271-9. PubMed ID: 9412783
[TBL] [Abstract][Full Text] [Related]
2. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
Howell N; Oostra RJ; Bolhuis PA; Spruijt L; Clarke LA; Mackey DA; Preston G; Herrnstadt C
Am J Hum Genet; 2003 Jun; 72(6):1460-9. PubMed ID: 12736867
[TBL] [Abstract][Full Text] [Related]
3. The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates.
Howell N; Smejkal CB; Mackey DA; Chinnery PF; Turnbull DM; Herrnstadt C
Am J Hum Genet; 2003 Mar; 72(3):659-70. PubMed ID: 12571803
[TBL] [Abstract][Full Text] [Related]
4. Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.
Hudson G; Keers S; Yu-Wai-Man P; Griffiths P; Huoponen K; Savontaus ML; Nikoskelainen E; Zeviani M; Carrara F; Horvath R; Karcagi V; Spruijt L; de Coo IF; Smeets HJ; Chinnery PF
Am J Hum Genet; 2005 Dec; 77(6):1086-91. PubMed ID: 16380918
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus.
Soini HK; Moilanen JS; Finnila S; Majamaa K
BMC Res Notes; 2012 Jul; 5():350. PubMed ID: 22780954
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass Surgery.
Kanagasundaram NS; Baudouin SV; Rowling S; Prabhu M; Dark JH; Goodship THJ; Chinnery PF; Hudson G
Sci Rep; 2019 Feb; 9(1):2279. PubMed ID: 30783114
[TBL] [Abstract][Full Text] [Related]
7.
Chinnery PF; Gomez-Duran A
Front Neurosci; 2018; 12():682. PubMed ID: 30369864
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial disorders and the eye.
Van Bergen NJ; Chakrabarti R; O'Neill EC; Crowston JG; Trounce IA
Eye Brain; 2011; 3():29-47. PubMed ID: 28539774
[TBL] [Abstract][Full Text] [Related]
9. Genetic background and climatic droplet keratopathy incidence in a Mapuche population from Argentina.
Schurr TG; Dulik MC; Cafaro TA; Suarez MF; Urrets-Zavalia JA; Serra HM
PLoS One; 2013; 8(9):e74593. PubMed ID: 24040292
[TBL] [Abstract][Full Text] [Related]
10. Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
Khan NA; Govindaraj P; Jyothi V; Meena AK; Thangaraj K
Mol Vis; 2013; 19():1282-9. PubMed ID: 23805034
[TBL] [Abstract][Full Text] [Related]
11. The neuro-ophthalmology of mitochondrial disease.
Fraser JA; Biousse V; Newman NJ
Surv Ophthalmol; 2010; 55(4):299-334. PubMed ID: 20471050
[TBL] [Abstract][Full Text] [Related]
12. Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese.
Ji Y; Jia X; Li S; Xiao X; Guo X; Zhang Q
Mol Vis; 2010 Mar; 16():416-24. PubMed ID: 20300564
[TBL] [Abstract][Full Text] [Related]
13. OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.
Pierron D; Ferré M; Rocher C; Chevrollier A; Murail P; Thoraval D; Amati-Bonneau P; Reynier P; Letellier T
BMC Med Genet; 2009 Jul; 10():70. PubMed ID: 19619285
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Ji Y; Zhang AM; Jia X; Zhang YP; Xiao X; Li S; Guo X; Bandelt HJ; Zhang Q; Yao YG
Am J Hum Genet; 2008 Dec; 83(6):760-8. PubMed ID: 19026397
[TBL] [Abstract][Full Text] [Related]
15. New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.
Pierron D; Rocher C; Amati-Bonneau P; Reynier P; Martin-Négrier ML; Allouche S; Batandier C; Mousson de Camaret B; Godinot C; Rotig A; Feldmann D; Bellanne-Chantelot C; Arveiler B; Pennarun E; Rossignol R; Crouzet M; Murail P; Thoraval D; Letellier T
BMC Med Genet; 2008 May; 9():41. PubMed ID: 18462486
[TBL] [Abstract][Full Text] [Related]
16. The role of mitochondrial haplogroups in primary open angle glaucoma.
Andrews R; Ressiniotis T; Turnbull DM; Birch M; Keers S; Chinnery PF; Griffiths PG
Br J Ophthalmol; 2006 Apr; 90(4):488-90. PubMed ID: 16547333
[TBL] [Abstract][Full Text] [Related]
17. Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
Carelli V; Achilli A; Valentino ML; Rengo C; Semino O; Pala M; Olivieri A; Mattiazzi M; Pallotti F; Carrara F; Zeviani M; Leuzzi V; Carducci C; Valle G; Simionati B; Mendieta L; Salomao S; Belfort R; Sadun AA; Torroni A
Am J Hum Genet; 2006 Apr; 78(4):564-74. PubMed ID: 16532388
[TBL] [Abstract][Full Text] [Related]
18. Increased variation in mtDNA in patients with familial sensorineural hearing impairment.
Lehtonen MS; Moilanen JS; Majamaa K
Hum Genet; 2003 Aug; 113(3):220-7. PubMed ID: 12802679
[TBL] [Abstract][Full Text] [Related]
19. The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness.
Torroni A; Cruciani F; Rengo C; Sellitto D; López-Bigas N; Rabionet R; Govea N; López De Munain A; Sarduy M; Romero L; Villamar M; del Castillo I; Moreno F; Estivill X; Scozzari R
Am J Hum Genet; 1999 Nov; 65(5):1349-58. PubMed ID: 10521300
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
