DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Segawa M, Nomura Y, Nishiyama N.
Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease).
Ann Neurol 2003;
54 (Suppl. 06) S32-S45
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.