Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene. Issue 12 (1st December 2002)

Record Type:: Journal Article
Title:: Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene. Issue 12 (1st December 2002)
Main Title:: Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene
Authors:: del Castillo, F J
Villamar, M
Moreno-Pelayo, M A
Almela, J J
Morera, C
Adiego, I
Moreno, F
del Castillo, I
Abstract:
Is Part Of:: Journal of medical genetics. Volume 39:Issue 12(2002)
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 12(2002)
Issue Display:: Volume 39, Issue 12 (2002)
Year:: 2002
Volume:: 39
Issue:: 12
Issue Sort Value:: 2002-0039-0012-0000
Page Start:: e82
Page End:: e82
Publication Date:: 2002-12-01
Subjects:: 7510T>C mutation -- genotype-phenotype correlation -- mitochondrial tRNASer(UCN) gene -- non-syndromic hearing impairment
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.39.12.e82 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 18079.xml