All individuals with variants in gene PDXK

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00183315 ASHG2018-P1122 Chelban ASHG2018 P1122 families - - - - - 1 - - neuropathy, peripheral severe primary axonal peripheral neuropathy, optic atrophy, blindness, severe muscle weakness/wasting, wheelchair-bound 1 1 Johan den Dunnen
00474810 - Delague V, submitted, PubMed: Megarbane 2022 2 families, 4 affected - - Lebanon - - - - - NMD - 1 4 Johan den Dunnen
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