Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene

Journal article

Peer reviewed

Alanoud Aldrees, Ehab Abdelkader, Hussain Al-Habboubi, Huda Alrwebah, Zuhair Rahbeeni and Patrik Schatz

Ophthalmic genetics, Vol.40(1), pp.77-79

02/01/2019

PMID: 30488743

Abstract

Cell Cycle Proteins - genetics

Child

Child, Preschool

Female

Homozygote

Humans

Male

Mutation

Retinal Dystrophies - genetics

Retinal Dystrophies - pathology

Young Adult

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Title: Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
Creators - without role: Alanoud Aldrees - King Abdulaziz Medical City
Ehab Abdelkader - Menoufia University
Hussain Al-Habboubi - e Ohud Hospital , Madinah , Kingdom of Saudi Arabia
Huda Alrwebah - King Abdulaziz Medical City
Zuhair Rahbeeni - f King Faisal Hospital , Riyadh , Kingdom of Saudi Arabia.
Patrik Schatz - Lund University
Publication Details: Ophthalmic genetics, Vol.40(1), pp.77-79
Identifiers: 9920588008331
Academic Unit: King Abdulaziz University; King Saud Bin Abdulaziz University for Health Sciences
Language: English
Resource Type: Journal article