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

A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.

The British journal of dermatology - 1 Jan 2005

Suzuki T, Inagaki K, Fukai K, Obana A, Lee S-T, Tomita Y

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 Antigens, Neoplasm
Share to Asian People
Share to Child

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Membrane Transport Proteins

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 15656822
DOI: 10.1111/j.1365-2133.2005.06403.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.PMID 15656822Read ↗

OCA4: evidence for a founder effect for the p.D157N mutation of the MATP gene in Japanese and Korean.Semantic proximity Read ↗

Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan.Semantic proximity Read ↗

Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.Semantic proximity Read ↗

Two novel splice mutations of P gene in a Thai-Chinese patient with oculocutaneous albinism type II (OCA2).Semantic proximity Read ↗

Two novel mutations detected in Japanese patients with oculocutaneous albinism.Semantic proximity Read ↗

[Analysis of P gene variations among fourteen patients with oculocutaneous albinism type II].Semantic proximity Read ↗

[Mutations and polymorphisms of the P gene associated with oculocutaneous albinism type II].Semantic proximity Read ↗

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2).Semantic proximity Read ↗

Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4.Semantic proximity Read ↗

[A new form of Oculocutaneous albinism, OCA4].Semantic proximity Read ↗

A novel mutation (delAACT) in the tyrosinase gene in a Cameroonian black with type 1A oculocutaneous albinism.Semantic proximity Read ↗

Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.Semantic proximity Read ↗

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