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Congenital myasthenic syndrome in cattle due to homozygosity for a truncating mutation in the acetylcholine receptor (AChR) epsilon-subunit gene

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons80526

Sieb,  J. P.
Max Planck Institute of Psychiatry, Max Planck Society;

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Sieb, J. P., Kraner, S., Thompson, P. N., & Steinlein, O. K. (2003). Congenital myasthenic syndrome in cattle due to homozygosity for a truncating mutation in the acetylcholine receptor (AChR) epsilon-subunit gene. In M. A. Agius (Ed.), Myasthenia gravis and related disorders: biochemical basis for disease of the neuromuscular junction (pp. 125-127). New York: New York Acad. of Sciences.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-9FE7-9
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