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Congenital disorder of glycosylation type Ia: Heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency

✍ Scribed by Shanti, B.; Silink, M.; Bhattacharya, K.; Howard, N. J.; Carpenter, K.; Fietz, M.; Clayton, P.; Christodoulou, J.


Book ID
120515038
Publisher
Springer
Year
2009
Tongue
English
Weight
250 KB
Volume
32
Category
Article
ISSN
0141-8955

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