Hypothesis

1 Matching Annotations

Last 7 days
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up

1
1. Vibhor 26 Jul 2026
  
  in read_only_demo_group
  
  Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up
  
  PMID: 31819343
  
  Gene: ABCA4
  
  HGNC ID: 34
  
  Gene:ABCA4 General PMID:31819343 HGNC:34 automated_hgnc:34 automated_hgnc_source:hgnc_tag ClinGen ABCA4 Annotations
Visit annotations in context

Tags

automated_hgnc:34

HGNC:34

General

Gene:ABCA4

ClinGen ABCA4 Annotations

automated_hgnc_source:hgnc_tag

PMID:31819343

Annotators

Vibhor

URL

pmc.ncbi.nlm.nih.gov/articles/PMC6887784/