Reactome | Lammens, M

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created	[InstanceEdit:4719368] Jassal, B, 2013-10-18
dbId	4719358
displayName	Lammens, M
firstname	Martin
initial	M
publications	[LiteratureReference:4755618] Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation [LiteratureReference:5609943] Multiple phenotypes in phosphoglucomutase 1 deficiency [LiteratureReference:4719349] Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
schemaClass	Person
surname	Lammens

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