All individuals with variants in gene GRM7

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00441568 B00APFY PubMed: Boucher 2020 - - - France - - - - - HL - 1 1 Johan den Dunnen
00467799 Fam014PatBAB6708/709 PubMed: Charng 2016 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M yes Saudi Arabia - - - - - NDD developmental delay, seizures, axial hypotonia, cortical atrophy, thin corpus callosum, hypomyelination, cerebellar volume loss, microcephaly 1 2 Johan den Dunnen
00467804 FamWGLPatBAB8506/brother PubMed: Charng 2016 family, affected sister/brothes, unaffected heterozygous carrier parents - - Saudi Arabia - - - - - NDD developmental delay, profound hypotonia, profound intellectual disability, hypomyelination, seizure, cortical atrophy, abnormal corpus callosum, cerebellar volume loss, microcephaly 2 2 Johan den Dunnen
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