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 frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis

19 Apr 2006

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 Carbohydrate Chemistry and Synthesis
Share to Glycosylation and Glycoproteins Research
Share to Lysosomal Storage Disorders Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16621647
DOI: 10.1016/j.ymgme.2006.02.016

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 frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosisPMID 16621647Read ↗

A novel CLN2/TPP1 mutation in a patient with late infantile neuronal ceroid lipofuscinosis.Semantic proximity Read ↗

Neuronal Ceroid Lipofuscinosis-Like Disorder in a Dachshund with Sequence Variants in Lysosome-Related GenesSemantic proximity Read ↗

A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs☆Semantic proximity Read ↗

A Missense Mutation in Canine <i>CLN6</i> in an Australian Shepherd with Neuronal Ceroid LipofuscinosisSemantic proximity Read ↗

A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestrySemantic proximity Read ↗

Juvenile-onset neuronal ceroid lipofuscinosis (CLN1) disease with a novel deletion and duplication in the PPT1 gene.Semantic proximity Read ↗

A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis.Semantic proximity Read ↗

A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosisSemantic proximity Read ↗

A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis.Semantic proximity Read ↗

Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 diseaseSemantic proximity Read ↗

A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund.Semantic proximity Read ↗

Neuronal Ceroid Lipofuscinosis-Like Disorder in a Petit Bleu de Gascogne Dog with Sequence Variants in AP3B1 and TRAPPC9Semantic proximity Read ↗

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