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

Sieb, J. P.; Kraner, S.; Thompson, P. N.; Steinlein, O. K.

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

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