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

Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.

Movement disorders : official journal of the Movement Disorder Society - 1 Jul 2011

Ormazabal Aida, Serrano Mercedes, Garcia-Cazorla Angels, Campistol Jaume, Artuch Rafael, Castro de Castro Pedro, Barredo-Valderrama Estíbaliz, Armstrong Judith, Toma Claudio, Cormand Bru

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 Antiparkinson Agents
Share to Drug Combinations
Share to Homovanillic Acid

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

Share to Levodopa

Share to Movement Disorders

Share to Sequence Deletion

Share to Tyrosine 3-Monooxygenase

Share to Video Recording

Source

Identifiers

PMID: 21465550
DOI: 10.1002/mds.23564

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.PMID 21465550Read ↗

Novel missense mutation in the phenylalanine hydroxylase gene leading to complete loss of enzymatic activity.Semantic proximity Read ↗

Mutations of the phenylalanine hydroxylase gene in mild hyperphenylalaninemia: a novel mutation in exon 3.Semantic proximity Read ↗

A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndromeSemantic proximity Read ↗

Biochemical and Molecular Genetic Characteristics of the Severe Form of Tyrosine Hydroxylase DeficiencySemantic proximity Read ↗

R233H mutation in patients with tyrosine hydroxylase deficiency and corresponding phenotypes: a study of four cases and literature review.Semantic proximity Read ↗

Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movementsSemantic proximity Read ↗

A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).Semantic proximity Read ↗

Mild phenotype in a patient with a de-novo 2.9-Mb interstitial deletion at 13q12.11.Semantic proximity Read ↗

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