Associated Papers
Linking Protein Stability to Pathogenicity: Predicting Clinical Significance of Single-Missense Mutations in Ocular Proteins Using Machine Learning.
Majid I et al.
International Journal of Molecular Sciences, 2024
39519200 (PubMed )
Supplement: ijms-25-11649-s001.zip › ijms-3279427-supplementary.pdf
PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing.
Makay P et al.
American Journal of Medical Genetics. Part A, 2022
Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa.
Oh JK et al.
Orphanet Journal of Rare Diseases, 2019
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.
Pehlivan D et al.
American Journal of Human Genetics, 2019
New macular findings in individuals with biallelic KLHL7 gene mutation.
Heng LZ et al.
Bmj Open Ophthalmology, 2019
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Angius A et al.
American Journal of Human Genetics, 2016
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