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Congenital Disorder of Glycosylation Type 1B

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Congenital Disorder of Glycosylation Type 1B

Explore clinical trials studying Congenital Disorder of Glycosylation Type 1B. Study availability and eligibility vary by location and protocol.

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Congenital Disorder of Glycosylation Type 1B trial results

Active, Not Recruiting

Early Check: Expanded Screening in Newborns

NCT03655223

Conditions: 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
Locations: RTI International Research Triangle Park, North Carolina, United States

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