DOI:
10.1055/s-00000019
Fortschritte der Neurologie · Psychiatrie
LinksClose Window
References
Chambliss K, Hinson D, Trettel F et al.
Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxy aciduria).
Am J Med Gen 1998;
63: 399-408
We do not assume any responsibility for the contents of the web pages of other providers.