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G.P.1.05 RYR1 is a common cause of congenital fibre type disproportion with ptosis, ophthalmoplegia, scoliosis and pronounced axial muscle weakness

✍ Scribed by N.F. Clarke; N. Monnier; R.L.L. Smith; A.J. Kornberg; M.A. Farrell; L. Waddell; S. Cooper; J. Lunardi; K.N. North


Book ID
116793954
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
43 KB
Volume
19
Category
Article
ISSN
0960-8966

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