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Glycogen branching enzyme deficiency in an infant with severe congenital hypotonia: an emerging diagnosis of muscle weakness in the perinatal period

✍ Scribed by Cecilia Jimenez-Mallebrera; Andres Nascimento; Victoria Cusi; Joan Ramon Corbera; Marie-Odile Rolland; Rosaline Froissart; Montse Olivé; Isidro Ferrer; Jaume Colomer


Book ID
108780712
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
594 KB
Volume
54
Category
Article
ISSN
0309-0167

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