All individuals with variants in gene AGTPBP1

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00301740 18DG0160 PubMed: Maddirevula 20198 - - - - - - - - - ? Cerebellar hypoplasia and lower motor neuron degeneration 1 1 Johan den Dunnen
00390068 Pat15 PubMed: Kritioti 2021 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Cyprus Greece - - - - ? deceased; global developmental delay, intellectual disability, failure to thrive, cerebellar atrophy, microcephaly, tremors, chilblains, erythroderma, feeding difficulties, hypotonia, seizures, spinal muscular atrophy, death in childhood 1 1 Johan den Dunnen
00433032 - - - M yes Egypt - - - - - CONDCA - 1 1 Alaaeldin Fayez
00433034 - - - M yes Egypt - - - - - CONDCA - 1 1 Alaaeldin Fayez
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.