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A common founder mutation in FKRP causes limb girdle muscular dystrophy type 21 (LGMD21) in both Hutterite and European populations

Lookup NU author(s): Professor Volker StraubORCiD, Emerita Professor Katherine Bushby

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Author(s): Frosk P, Greenberg CR, Poulin A, Lamont R, Nylen E, Zaik M, Straub V, Bushby K, Frappier D, Roslin NM, Morgan K, Fujiwara TM, Wrogemann K

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: American Journal of Human Genetics: Annual Meeting of the American Society of Human Genetics

Year of Conference: 2003

Pages: 388 abstract no. 1275

ISSN: 0002-9297

Publisher: Cell Press

Library holdings: Search Newcastle University Library for this item

ISBN: 15376605

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