DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
O'Connor E, Töpf A, Müller JS. , et al.
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome.
Brain 2016;
139 (Pt 8): 2143-2153
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.