Back to School: How biopharma can reboot drug development. Access exclusive analysis here

KIF5A mutations a cause of ALS

In a paper published in Neuron, an international consortium of researchers identified loss-of-function mutations in the kinesin family member 5A (KIF5A) gene as a cause of amyotrophic lateral sclerosis through large-scale genome studies combined with exome

Read the full 365 word article

Trial Subscription

Get a two-week free trial subscription to BioCentury

SIGN UP

Article Purchase

This article may not be distributed to non-subscribers
More Info >PURCHASE