Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency).

Authors :: Schollen, E.
Frank, C.G.
Keldermans, L.
Reyntjens, R.
Grubenmann, C.E.
Clayton, P.T.
Winchester, B.G.
Smeitink, J.A.M.
Wevers, R.A.
Aebi, M.
Hennet, T.
Matthijs, G.
Schollen, E.
Frank, C.G.
Keldermans, L.
Reyntjens, R.
Grubenmann, C.E.
Clayton, P.T.
Winchester, B.G.
Smeitink, J.A.M.
Wevers, R.A.
Aebi, M.
Hennet, T.
Matthijs, G.
Source :: Journal of Medical Genetics; 550; 556; 0022-2593; 7; 41; ~Journal of Medical Genetics~550~556~~~0022-2593~7~41~~
Publication Year :: 2004
Abstract: Contains fulltext : 57365.pdf (publisher's version ) (Closed access)

Database :: OAIster
Journal :: Journal of Medical Genetics; 550; 556; 0022-2593; 7; 41; ~Journal of Medical Genetics~550~556~~~0022-2593~7~41~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284098565
Document Type :: Electronic Resource

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