Login / Signup
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene.
Alanoud Aldrees
Ehab Abdelkader
Hussain Al-Habboubi
Huda Alrwebah
Zuhair Rahbeeni
Patrik Schatz
Published in:
Ophthalmic genetics (2018)
Keyphrases
</>
optical coherence tomography
diabetic retinopathy
intellectual disability
early onset
genome wide
copy number
genome wide identification
dna methylation
gene expression
autism spectrum disorder
transcription factor
genome wide analysis