Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”
Main Authors: | Ruth Helen Walker, Robert Alexander Hegele, Adrian Danek |
---|---|
Format: | Article |
Language: | English |
Published: |
Korean Movement Disorder Society
2021-09-01
|
Series: | Journal of Movement Disorders |
Online Access: | http://www.e-jmd.org/upload/jmd-20145.pdf |
Similar Items
-
A New Allelic Variant in the Gene in a Patient with Incomplete HARP Syndrome
by: Myriam Ley Martos, et al.
Published: (2020-09-01) -
Bi-Allelic Mutations in Zebrafish <i>pank2</i> Gene Lead to Testicular Atrophy and Perturbed Behavior without Signs of Neurodegeneration
by: Luca Mignani, et al.
Published: (2022-10-01) -
Case report: Novel compound heterozygous variants in the PANK2 gene in a Chinese patient diagnosed with ASD and ADHD
by: Siqi Dong, et al.
Published: (2023-04-01) -
The harp lesson /
by: 262936 Tennant, Emma
Published: (2005) -
Generation and Validation of an Anti-Human PANK3 Mouse Monoclonal Antibody
by: Sunada Khadka, et al.
Published: (2022-09-01)