GPI-anchor biosynthesis

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GPI-anchor biosynthesis

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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GPI-anchor_biosynthesis

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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Other names: GPI-anchor_biosynthesis

Inherited glycophosphatidylinositol deficiency variant database.

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Inherited glycophosphatidylinositol deficiency variant database and analysis of pathogenic variants
PMID: 31127708

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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• Inherited glycophosphatidylinositol deficiency variant database and analysis of pathogenic variants PubMed citations: 3.

  3 articles citing: Inherited glycophosphatidylinositol deficiency variant database and analysis of pathogenic variants

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  Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis. PMID:33392778

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  Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ: Report of seven new subjects and review of the literature. PMID:32588908

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  Early infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutations. PMID:32042915

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neurology

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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genetic variation

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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genotype and phenotype

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:24.956334

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neurology genetic variation genotype and phenotype