Associated Papers
An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.
Baskar D et al.
Journal of Neuromuscular Diseases, 2025
Progress on the study of Popeye domain-containing 3 (POPDC3) in malignancies and striated muscle function and homeostasis.
Sun CC et al.
Clinical Genetics, 2023
A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype.
De Ridder W et al.
Neuromuscular Disorders : Nmd, 2023
A novel splice site variant in the POPDC3 causes autosomal recessive limb-girdle muscular dystrophy type 26.
Zhang L et al.
Clinical Genetics, 2022
Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26.
Ullah A et al.
The Journal of Gene Medicine, 2022
ConVarT: a search engine for matching human genetic variants with variants from non-human species.
Pir MS et al.
Nucleic Acids Research, 2022
34718716 (PubMed )
Supplement: gkab939_supplemental_files.zip › Table_S14.xls › human_pat_mouse_unk_orthovar_14
The Role of POPDC Proteins in Cardiac Pacemaking and Conduction.
Gruscheski L et al.
Journal of Cardiovascular Development and Disease, 2021
Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.
Fareed M et al.
Frontiers in Genetics, 2021
34113375 (PubMed )
Supplement: Data_Sheet_1.pdf
POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy.
Vissing J et al.
Annals of Neurology, 2019
Select a paper to view details