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Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele

✍ Scribed by Natalia Garcia-Angarita; Janbernd Kirschner; Mandy Heiliger; Christian Thirion; Maggie C. Walter; Susanne Schnittfeld-Acarlioglu; Matthias Albrecht; Klaus Müller; Dagmar Wieczorek; Hanns Lochmüller; Sabine Krause


Book ID
116793903
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
501 KB
Volume
19
Category
Article
ISSN
0960-8966

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