Search

Search Constraints

You searched for: Author/Creator Seta, N

Search Results

2. A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases. Issue 1 (1st January 2001)

3. Conotruncal heart defects in three patients with congenital disorder of glycosylation type Ia (CDG Ia). Issue 4 (8th April 2009)

4. Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations. Issue 11 (2nd August 2010)

5. Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type Ib. Issue 11 (1st November 2002)