Varaico: Literature-Extracted Genetic Variants

Gene:HPDL
Variant:p.L217P
Back to variants list

HPDL

NM_032756.4:p.L217P

Associated Papers

HPDL Variant Type Correlates With Clinical Disease Onset and Severity.

Lee EH et al.

Annals of Clinical and Translational Neurology, 2025

Quantitative natural history modeling of HPDL-related disease based on cross-sectional data reveals genotype-phenotype correlations.

Alecu JE et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025

Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.

Zhi Y et al.

Cns Neuroscience & Therapeutics, 2025

39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG83

Two novel heterozygous HPDL variants in a Chinese family with a neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities.

Ma Y et al.

Gene, 2025

Concurrent Preimplantation Genetic Testing and Competence Assessment of Human Embryos by Transcriptome Sequencing.

Wang Y et al.

Advanced Science (weinheim, Baden-wurttemberg, Germany), 2024

38900059 (PubMed )
Supplement: ADVS-11-2309817-s002.xlsx › Table_S5

A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review.

Kojima F et al.

Neurogenetics, 2024

HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.

Wang Y et al.

Molecular Genetics & Genomic Medicine, 2022

Case Report: Two Families With HPDL Related Neurodegeneration.

Micule I et al.

Frontiers in Genetics, 2022

Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.

Barbosa P et al.

Frontiers in Cardiovascular Medicine, 2022

36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S6

Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.

Wiessner M et al.

Brain : a Journal of Neurology, 2021

Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL.

Morgan NV et al.

Brain Communications, 2021

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."