RESEARCHDIAGNOSTICSTRANSLATIONOUTREACH
 
Paper Detail
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Quelhas D, Quental R, Vilarinho L, Amorim A, Azevedo L
Congenital disorder of glycosylation type Ia: searching for the origin of common mutations in PMM2. Annals of human genetics 71: 348-53, 2007.  [Article] 
 doi: 10.1111/j.1469-1809.2006.00334.x PMID: 17166182.
 
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@ 2014 Ipatimup Institute of Molecular Pathology and Immunology of the University of Porto
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