Chronic stridor as an early presentation of congenital myasthenic syndrome due to RAPSN mutation - ORA - Oxford University Research Archive

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Chronic stridor as an early presentation of congenital myasthenic syndrome due to RAPSN mutation

Publication status:: Published

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APA Style

Mewasingh, L., Hussein, N., Jayawant, S., Newsom-Davis, J., & Beeson, D. (2016). Chronic stridor as an early presentation of congenital myasthenic syndrome due to RAPSN mutation. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 48, 30–30.

MLA Style

Mewasingh, L., et al. “Chronic Stridor as an Early Presentation of Congenital Myasthenic Syndrome Due to RAPSN Mutation.” DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, vol. 48, 2016, pp. 30–30.

Chicago Style

Mewasingh, L, N Hussein, S Jayawant, J Newsom-Davis, and D Beeson. 2016. “Chronic Stridor as an Early Presentation of Congenital Myasthenic Syndrome Due to RAPSN Mutation.” DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 48: 30–30.
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+ Mewasingh, L More by this author

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Author

+ Hussein, N More by this author

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Author

+ Jayawant, S More by this author

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+ Newsom-Davis, J More by this author

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+ Beeson, D More by this author

Institution:

University of Oxford

Division:

MSD

Department:

RDM

Sub department:

Weatherall Insti. of Molecular Medicine

Role:

Author

Bibliographic Details

Journal:: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
Volume:: 48
Pages:: 30-30
Publication date:: 2006-01-01
ISSN:: 0012-1622
Source identifiers:: 324392

Item Description

Pubs id:: pubs:324392
UUID:: uuid:a51fb9c6-5f80-455d-a5be-e98a295b0251
Local pid:: pubs:324392
Deposit date:: 2012-12-19

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Copyright date:: 2006

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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