HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia

HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia

10.1111/cge.12030

Saved in:
Bibliographic Details
Main Author: Aminkeng, F
Other Authors: MEDICINE
Format: Editorial
Language:English
Published: WILEY-BLACKWELL 2022
Subjects:
Science & Technology
Life Sciences & Biomedicine
Genetics & Heredity
Online Access:https://scholarbank.nus.edu.sg/handle/10635/235312
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: National University of Singapore
Language: English
Description
Summary:10.1111/cge.12030

Similar Items