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

Pseudoperiodic electroencephalogram pattern in a child with late infantile neuronal ceroid lipofuscinoses with a novel CLN6 mutation.

Neurology India - 1 Jan 2000

Jain Puneet, Sharma Suvasini, Aneja Satinder

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 Child
Share to Electroencephalography
Share to Membrane Proteins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neuronal Ceroid-Lipofuscinoses

Source

Identifiers

PMID: 27147172
DOI: 10.4103/0028-3886.181551

Genes

CLN6

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 · 12 closest

Pseudoperiodic electroencephalogram pattern in a child with late infantile neuronal ceroid lipofuscinoses with a novel CLN6 mutation.PMID 27147172Read ↗

Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations.Semantic proximity Read ↗

Gene symbol: CLN6. Disease: Neuronal ceroid lipofuscinosis, late infantile.Semantic proximity Read ↗

Gene symbol: CLN6. Disease: Neuronal ceroid lipofuscinosis, late Infantile.Semantic proximity Read ↗

[Neuronal ceroid lipofuscinosis. Type 6 late infantile variant in two compound heterozygous siblings with novel mutations].Semantic proximity Read ↗

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.Semantic proximity Read ↗

Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion.Semantic proximity Read ↗

CLN6-related continuum phenotype caused by aberrant splicing.Semantic proximity Read ↗

[Pitfalls in the clinical and electroencephalographic diagnosis of ceroid lipofuscinosis].Semantic proximity Read ↗

Chorea in Late-Infantile Neuronal Ceroid Lipofuscinosis: An Atypical Presentation.Semantic proximity Read ↗

First Japanese variant of late infantile neuronal ceroid lipofuscinosis caused by novel CLN6 mutations.Semantic proximity Read ↗

Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations.Semantic proximity Read ↗

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

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