Congenital Disorders of Glycosylation: Diagnostic steps - ERNDIM
Congenital Disorders of Glycosylation: Diagnostic steps - ERNDIM
Congenital Disorders of Glycosylation: Diagnostic steps - ERNDIM
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Group 2: 14/21 patients with cutis laxa phenotype<br />
4<br />
3<br />
2<br />
1<br />
2<br />
1<br />
0<br />
group 2: ApoCIII-1
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