ALS is a motor neuron disease, which is a group of neurological disorders that selectively affect motor neurons with secondary damage to muscles. In a normal body, there is a motor nervous system that works in an orderly manner.
Read More ›
Cyagen assists in the research of rare diseases and provides various mouse/rat models, including the SYNGAP1-related rodent animal models. This article focuses on the gene SYNGAP1 and rare disease MRD5, aiming to help interested researchers continue to build on scientific literature and knowledge.
Read More ›
The ERCC6 gene is located on human chromosome 10, 10q11, with a total length of 104.7 kb, a total of 23 exons, and 1493 amino acids. Mutations in the ERCC6 gene are closely related to Cockayne syndrome B (CSB).
Read More ›
We use cookies to ensure that we give you the best experience on our website. To learn about how we
keep your information safe, view our Privacy Policy.
OKPrivacy policy
