Associated Papers
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies.
Hadjipanteli A et al.
Genes, 2024
38255008 (PubMed )
Supplement: genes-15-00119-s001.zip › All_rare_variants_for_fetus_1__manuscript_supplementary_material_.xlsx › Variant_details
Reply: Segregation of ATP10B variants in families with autosomal recessive Parkinsonism.
Smolders S et al.
Acta Neuropathologica, 2020
Segregation of ATP10B variants in families with autosomal recessive parkinsonism.
Tesson C et al.
Acta Neuropathologica, 2020
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Martin S et al.
Acta Neuropathologica, 2020
32172343 (PubMed )
Supplement: 401_2020_2145_MOESM1_ESM.pdf
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