![](/img/cover-not-exists.png)
Succinic Semialdehyde Dehydrogenase Deficiency in a Chinese Boy: A Novel ALDH5A1 Mutation With Severe Phenotype
Tay, C. G., Ariffin, H., Yap, S., Rahmat, K., Sthaneshwar, P., Ong, L. C.Volume:
30
Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073814540523
Date:
June, 2015
File:
PDF, 502 KB
english, 2015