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  1. Congenital disorders of glycosylation type Ig is defined by a deficiency in...

    Type I congenital disorders of glycosylation (CDG I) are diseases presenting multisystemic lesions including central and peripheral nervous system deficits. The disease is characterized by under-glycosylated serum glycoproteins and is caused by

    http://iris.ucl.ac.uk/iris/publication/242291/2

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