DOI:
10.1055/s-00034916
Nervenheilkunde
LinksClose Window
References
Huzé C. et al.
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.
Am J Hum Genet 2009;
85 (02) 155-67.
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.