Download from app store
We have detected that you are using an Ad Blocker.
PracticeUpdate is free to end users but we rely on advertising to fund our site. Please consider supporting PracticeUpdate by whitelisting us in your ad blocker.
We have sent a message to the email address you have provided, . If this email is not correct, please update your settings with your correct address.
The email address you provided during registration, , does not appear to be valid. Please update your settings with a valid address before to continue using PracticeUpdate.
Please provide your AHPRA Number to ensure that you are given the correct level of access to our site.
 
Sign in
Join now
story of the week
Published in Von Hippel-Lindau Disease

Journal Scan / Research · December 01, 2022

Elongin C–Associated von Hippel–Lindau Disease

Human Molecular Genetics

 

 Save  Recommend
 Share

Additional Info

Human Molecular Genetics
Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau disease
Hum Mol Genet 2022 Aug 23;31(16)2728-2737, A Andreou, B Yngvadottir, L Bassaganyas, G Clark, E Martin, J Whitworth, AJ Cornish, , RS Houlston, P Rich, C Egan, SV Hodgson, AY Warren, K Snape, ER Maher

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Further Reading

Recently Updated