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 spectrum of mutational damage to the phenylalanine hydroxylase gene in patients with phenylketonuria in St. Petersburg].

Doklady Akademii nauk - 1 Feb 1995

Baranovskaia S S, Shevtsov S P, Maksimova S P, Kuz'min A I, Shvarts E I

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 Base Sequence
Share to DNA Primers
Share to Genetics, Population
Share to Molecular Sequence Data

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

Share to Phenylalanine Hydroxylase

Share to Phenylketonurias

Share to Polymorphism, Single-Stranded Conformational

Share to Russia

Source

Identifiers

PMID: 7735096

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[The spectrum of mutational damage to the phenylalanine hydroxylase gene in patients with phenylketonuria in St. Petersburg].PMID 7735096Read ↗

[Catalog of mutations of the phenylalanine hydroxylase gene].Semantic proximity Read ↗

The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg.Semantic proximity Read ↗

Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark.Semantic proximity Read ↗

[Molecular genetics of phenylketonuria in Novosibirsk Region].Semantic proximity Read ↗

[Mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Tianjin and surrounding areas of Northern China].Semantic proximity Read ↗

[Mutations causing hereditary hyperphenylalaninemia].Semantic proximity Read ↗

[Mutation in the structure of exon 7 of the phenylalanine hydroxylase in phenylketonuria patients from the Novosibirsk area].Semantic proximity Read ↗

[The mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Henan province].Semantic proximity Read ↗

[Mutational spectrum of phenylalanine hydroxylase gene and identification of novel mutations in patients with hyperphenylalaninemia in Jiangsu province].Semantic proximity Read ↗

[Phenylketonuria (phenylalanine hydroxylase deficiency)].Semantic proximity Read ↗

Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutations.Semantic proximity Read ↗

Mutational spectrum of phenylketonuria in Ireland.Semantic proximity Read ↗

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