z-logo
open-access-imgOpen Access
Commentary: Heteroplasmy in maternally inherited diabetes and deafness
Author(s) -
Bhavik Panchal,
Ketan Saoji
Publication year - 2019
Publication title -
indian journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 51
eISSN - 1998-3689
pISSN - 0301-4738
DOI - 10.4103/ijo.ijo_1296_19
Subject(s) - heteroplasmy , mitochondrial dna , melas syndrome , medicine , lactic acidosis , mitochondrial disease , genetics , mitochondrial encephalomyopathies , kearns–sayre syndrome , mitochondrial myopathy , mitochondrial encephalomyopathy , sensorineural hearing loss , mutation , chronic progressive external ophthalmoplegia , hearing loss , biology , audiology , gene

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom