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G.P.14.13 Phenotypic characterization of two unrelated UK families with X-linked myopathy and an identical mutation in the FHL1 gene

✍ Scribed by A. Sarkozy; K. Bushby; D. Hilton-Jones; C.F. Dougan; H. Lochmüller; C. Windpassinger; V. Straub


Book ID
116793736
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
50 KB
Volume
18
Category
Article
ISSN
0960-8966

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