All individuals with variants in gene PNPLA8

2 entries on 1 page. Showing entries 1 - 2.
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     
00024128 - PubMed: Saunders 2015, Journal: Saunders 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents F no United States - - - - - MYOP suspected mitochondrial myopathy manifested as progressive muscle weakness, hypotonia, seizures, poor weight gain, lactic acidosis 2 1 Carol Saunders
00467285 CMH193 PubMed: Soden 2014 family, 1 affected - - United States - - - - - ? - 2 1 Johan den Dunnen
Legend   How to query  


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