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GPIHBP1

HGNC ↗

Familial chylomicronaemia syndrome (GPIHBP1)

1 article(s) in the watch · Bioinformatics & AI

Curated publications

6/10

Resolving a complex GPIHBP1 exons 3-4 deletion adjacent to low-complexity repeats using adaptive sampling long-read sequencing in familial chylomicronaemia.

Familial chylomicronaemia syndrome (GPIHBP1)

Bio20 May 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.