Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on funduscopic appearance in an asymptomatic patient.

The British journal of ophthalmology - 1 Apr 2012

Strauss Danielle Savitsky, Freund K Bailey

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Deafness
Share to Diabetes Mellitus, Type 2
Share to Diagnosis, Differential
Share to DNA, Mitochondrial
Share to Mitochondria
Share to Mitochondrial Diseases
Share to Ophthalmoscopy
Share to Retina

Source

Identifiers

PMID: 22049499
DOI: 10.1136/bjophthalmol-2011-300004

Provenance

PubMed metadata and Literature Corpus relationships.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics