Literature DB >> 11424923

Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln.

S Finnilä, J Autere, M Lehtovirta, P Hartikainen, A Mannermaa, H Soininen, K Majamaa.   

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Year:  2001        PMID： 11424923      PMCID： PMC1734884          DOI： 10.1136/jmg.38.6.400

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

Review 1.  A possible role for mitochondrial dysfunction in migraine.

Authors:  S Stuart; L R Griffiths
Journal:  Mol Genet Genomics       Date:  2012-10-07       Impact factor: 3.291

2.  Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility.

Authors:  Shani Stuart; Miles C Benton; David A Eccles; Heidi G Sutherland; Larisa M Haupt; Rodney A Lea; Lyn R Griffiths
Journal:  Mol Genet Genomic Med       Date:  2017-01-17       Impact factor: 2.183

3.  A Pilot Mitochondrial Genome-Wide Association on Migraine Among Saudi Arabians.

Authors:  Lubna Al Asoom; Johra Khan; Ahmad Al Sunni; Nazish Rafique; Rabia Latif; Majed Alabdali; Sayed AbdulAzeez; J Francis Borgio
Journal:  Int J Gen Med       Date:  2022-07-21
  3 in total

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