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P.P.5 02 Muscle MRI in a family with congenital myopathy with cores and rods associated with a novel missense mutation in the ryanodine receptor 1 gene

✍ Scribed by M. von der Hagen; A.M. Kaindl; W. Kress; P. Mitzscherling; A. Hübner; C.R. Reible; G. Hahn; G. Stoltenburg-Didinger


Book ID
116792603
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
59 KB
Volume
16
Category
Article
ISSN
0960-8966

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