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

Kufor-Rakeb Syndrome/ Parkinson Disease Type 9.

Indian journal of pediatrics - 1 Mar 2020

Gowda Vykuntaraju K, Srinivasan Varunvenkat M, Shivappa Sanjay K

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, Preschool
Share to Developmental Disabilities
Share to India
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Parkinson Disease

Share to Parkinsonian Disorders

Share to Proton-Translocating ATPases

Source

Identifiers

PMID: 31933133
DOI: 10.1007/s12098-019-03167-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Kufor-Rakeb Syndrome/ Parkinson Disease Type 9.PMID 31933133Read ↗

Kufor-Rakeb syndrome: a cohort-based clinical, imaging and genetic profile.Semantic proximity Read ↗

Kufor-Rakeb Syndrome/PARK9: One Novel and One Possible Recurring Ashkenazi ATP13A2 Mutation.Semantic proximity Read ↗

History, genetic, and recent advances on Krabbe diseaseSemantic proximity Read ↗

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.Semantic proximity Read ↗

A Diagnostic Model for Parkinson’s Disease Based on Anoikis-Related GenesSemantic proximity Read ↗

[Genetic basis of sponadic Parkinson disease: common disease-multiple rare variants].Semantic proximity Read ↗

Krabbe Disease: Genetic Aspects and Progress toward TherapySemantic proximity Read ↗

Gene symbol: STK11. Disease: Peutz-Jeghers Syndrome.Semantic proximity Read ↗

Brugada syndrome 1992-2012: 20 years of scientific excitement, and more.Semantic proximity Read ↗

Early-Onset Dystonia, Exacerbation With Fever, and Striatal Signal Changes: Emerging Phenotype of DYT-PRKRA.Semantic proximity Read ↗

[Pelizaeus-Merzbacher disease(PMD)/spastic paraplegia 2(SPG2)].Semantic proximity Read ↗

Kufor-Rakeb Syndrome-Associated Psychosis: A Novel Loss-of-Function<i>ATP13A2</i>Variant and Response to TreatmentSemantic proximity Read ↗

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