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Nurulamin Abu Bakar
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Nurulamin Abu Bakar
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A mutation in mannose‐phosphate‐dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy
by
Walinka vanTol
,
Angel Ashikov
,
Eckhard Korsch
,
Nurulamin
Abu
Bakar
,
Michèl A. Willemsen
,
Christian Thiel
,
Dirk J. Lefeber
Published 2019-11-01
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