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A new phenotype of autosomal dominant nemaline myopathy

✍ Scribed by I.M.P. Gommans; B.G.M. van Engelen; H.J. ter Laak; H.G. Brunner; H. Kremer; M. Lammens; O.J.M. Vogels


Book ID
117669444
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
388 KB
Volume
12
Category
Article
ISSN
0960-8966

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