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pubmed.ncbi.nlm.nih.gov pubmed.ncbi.nlm.nih.gov

Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease

1
1. Vibhor 26 Jul 2026
  
  in read_only_demo_group
  
  Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease
  
  PMID: 19352439
  
  Gene: ABCA4
  
  HGNC ID: 34
  
  Gene:ABCA4 PMID: 19352439 General HGNC ID: 34 automated_hgnc:34 automated_hgnc_source:Gene_Name ClinGen ABCA4 Annotations
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automated_hgnc:34

PMID: 19352439

Gene:ABCA4

automated_hgnc_source:Gene_Name

ClinGen ABCA4 Annotations

General

HGNC ID: 34

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Vibhor

URL

pubmed.ncbi.nlm.nih.gov/19352439/