All individuals with variants in gene GCSH

3 entries on 1 page. Showing entries 1 - 3.
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     
00074415 - PubMed: Koyata 1991 - - no Japan - - - - - GCE one case glycine encephalopathy (605899), one case with NKH (deficiency of glycine decarboxylase) 1 2 Johan den Dunnen
00074416 - PubMed: Kure 2002 2-generation family, 1 affected, unaffected heterozygous carrier mother/brother M no Japan Asian >05y - - - GCE nonketotic hyperglycinemia (NKH), MRI no agenesis of corpus callosum, no delay in myelination; EEG neonatal burst suppression, currently normal on vitB6; severe intellectual disability, seizures responsive to vitB6 2 1 Johan den Dunnen
00324958 - - - F no India - 01y - - - glycine encephalopathy - 1 2 Anju Shukla
Legend   How to query  


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