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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-9FE7-9 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-9FE8-7

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Creators:
Sieb, J. P.¹, Author
Kraner, S., Author
Thompson, P. N., Author
Steinlein, O. K., Author

Affiliations:
1Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137

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Free keywords: South African Red-Brahman calves, domestic animals, sequence analysis, deletion, mutation

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Language(s): eng - English

Dates: Date issued: 2003

Publication Status: Issued

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Identifiers: eDoc: 121764
ISI: 000186107400013

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Title: Myasthenia gravis and related disorders: biochemical basis for disease of the neuromuscular junction

Source Genre: Book

Creator(s):
Agius, Mark A., Editor

Affiliations:
-

Publ. Info: New York : New York Acad. of Sciences

Pages: - Volume / Issue: - Sequence Number: - Start / End Page: 125 - 127 Identifier: -

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Title: Annals of the New York Academy of Sciences

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Pages: - Volume / Issue: 998 Sequence Number: - Start / End Page: - Identifier: ISSN: 0077-8923