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A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene

✍ Scribed by Pérez, Belén; Medrano, Celia; Ecay, Maria Jesus; Ruiz-Sala, Pedro; Martínez-Pardo, Mercedes; Ugarte, Magdalena; Pérez-Cerdá, Celia


Book ID
121636991
Publisher
Springer
Year
2012
Tongue
English
Weight
450 KB
Volume
36
Category
Article
ISSN
0141-8955

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