1. Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene. (1st March 2020) Authors: Al‐Hage, J.; Abbas, O.; Nemer, G.; Kurban, M. Journal: Clinical and experimental dermatology Issue: Volume 45:Number 2(2020) Page Start: 257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene. (4th September 2019) Authors: Al‐Hage, J.; Abbas, O.; Nemer, G.; Kurban, M. Journal: Clinical and experimental dermatology Issue: Volume 45:Number 2(2020) Page Start: 257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Unusual presentation of severe photosensitivity and neurodevelopmental delay in a consanguineous family. (12th March 2019) Authors: Al‐Hage, J.; Nemer, G.; Kassabian, P.; Kurban, M. Journal: Clinical and experimental dermatology Issue: Volume 45:Number 1(2020) Page Start: 117 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Unusual presentation of severe photosensitivity and neurodevelopmental delay in a consanguineous family. (1st January 2020) Authors: Al‐Hage, J.; Nemer, G.; Kassabian, P.; Kurban, M. Journal: Clinical and experimental dermatology Issue: Volume 45:Number 1(2020) Page Start: 117 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗