The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy

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Bibliographic Details
Main Authors:	Kristy Swiderski (Author), Audrey S. Chan (Author), Marco J. Herold (Author), Andrew J. Kueh (Author), Jin D. Chung (Author), Justin P. Hardee (Author), Jennifer Trieu (Author), Annabel Chee (Author), Timur Naim (Author), Paul Gregorevic (Author), Gordon S. Lynch (Author)
Format:	Book
Published:	The Company of Biologists, 2024-04-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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001	doaj_0b8d5a9dc15b471b9c11baee9e4ca30c
042			\|a dc
100	1	0	\|a Kristy Swiderski \|e author
700	1	0	\|a Audrey S. Chan \|e author
700	1	0	\|a Marco J. Herold \|e author
700	1	0	\|a Andrew J. Kueh \|e author
700	1	0	\|a Jin D. Chung \|e author
700	1	0	\|a Justin P. Hardee \|e author
700	1	0	\|a Jennifer Trieu \|e author
700	1	0	\|a Annabel Chee \|e author
700	1	0	\|a Timur Naim \|e author
700	1	0	\|a Paul Gregorevic \|e author
700	1	0	\|a Gordon S. Lynch \|e author
245	0	0	\|a The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy
260			\|b The Company of Biologists, \|c 2024-04-01T00:00:00Z.
500			\|a 1754-8403
500			\|a 1754-8411
500			\|a 10.1242/dmm.050502
546			\|a EN
690			\|a muscular dystrophy
690			\|a skeletal muscle
690			\|a bone
690			\|a pathophysiology
690			\|a preclinical
690			\|a genetic modifier
690			\|a Medicine
690			\|a R
690			\|a Pathology
690			\|a RB1-214
655	7		\|a article \|2 local
786	0		\|n Disease Models & Mechanisms, Vol 17, Iss 4 (2024)
787	0		\|n http://dmm.biologists.org/content/17/4/dmm050502
787	0		\|n https://doaj.org/toc/1754-8403
787	0		\|n https://doaj.org/toc/1754-8411
856	4	1	\|u https://doaj.org/article/0b8d5a9dc15b471b9c11baee9e4ca30c \|z Connect to this object online.