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

The molecular basis of type I (tyrosinase-deficient) human oculocutaneous albinism.

Pigment cell research - 1 Jan 1992

Giebel L B, Spritz R A

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 Albinism, Oculocutaneous
Share to Chromosomes, Human, Pair 11
Share to Consanguinity
Share to Ethnicity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Melanins

Share to Monophenol Monooxygenase

Source

Identifiers

PMID: 1409411
DOI: 10.1111/j.1600-0749.1990.tb00357.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The molecular basis of type I (tyrosinase-deficient) human oculocutaneous albinism.PMID 1409411Read ↗

Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1).Semantic proximity Read ↗

Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.Semantic proximity Read ↗

Molecular genetics of oculocutaneous albinism.Semantic proximity Read ↗

Molecular genetics of oculocutaneous albinism.Semantic proximity Read ↗

[Human oculocutaneous albinism. From clinical observation to molecular biology].Semantic proximity Read ↗

Oculocutaneous albinism type 1: the last 100 years.Semantic proximity Read ↗

Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.Semantic proximity Read ↗

Molecular basis of oculocutaneous albinism.Semantic proximity Read ↗

Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.Semantic proximity Read ↗

Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism.Semantic proximity Read ↗

The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): A model for understanding the molecular biology of melanin formation.Semantic proximity Read ↗

Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.Semantic proximity Read ↗

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