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

Molecular genetics of human visual pigments.

Annual review of genetics - 1 Jan 1992

Nathans J, Merbs S L, Sung C H, Weitz C J, Wang Y

Abstract excerpt

No abstract is available from the source.

Topics

Amino Acid Sequence
Color Vision Defects
Female
Humans
Male
Molecular Biology
Mutation
Retinal Pigments
Retinitis Pigmentosa
Rhodopsin

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1482119
DOI: 10.1146/annurev.ge.26.120192.002155

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular genetics of human visual pigments.PMID 1482119Read ↗

Visual pigments and inherited variation in human vision.Semantic proximity Read ↗

In the eye of the beholder: visual pigments and inherited variation in human vision.Semantic proximity Read ↗

The genetics of normal and defective color vision.Semantic proximity Read ↗

Genetics and physiology of color vision. A review.Semantic proximity Read ↗

Molecular analysis of human red/green visual pigment gene locus: relationship to color vision.Semantic proximity Read ↗

The genetics of human pigmentary disorders.Semantic proximity Read ↗

Visual function and risk genotypes in maternally inherited diabetes and deafness.Semantic proximity Read ↗

The genetic basis of human pigmentationSemantic proximity Read ↗

Molecular genetics of human retinal dystrophiesSemantic proximity Read ↗

Inherited disorders of pigmentation.Semantic proximity Read ↗

Molecular genetics of blindness.Semantic proximity Read ↗

Cone Opsins and Inherited Retinal Disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.