Increased risk of sensorineural hearing loss and migraine in patients witha rare mitochondrial DNA variant 4336A > G in tRNA(Gln)

Citation
S. Finnila et al., Increased risk of sensorineural hearing loss and migraine in patients witha rare mitochondrial DNA variant 4336A > G in tRNA(Gln), J MED GENET, 38(6), 2001, pp. 400-405
Citations number
30
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics
Journal title
JOURNAL OF MEDICAL GENETICS
ISSN journal
00222593 → ACNP
Volume
38
Issue
6
Year of publication
2001
Pages
400 - 405
Database
ISI
SICI code
0022-2593(200106)38:6<400:IROSHL>2.0.ZU;2-C