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Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry
Cahan, Eli M., Frick, Steven L.Volume:
14
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-019-1131-4
Date:
December, 2019
File:
PDF, 1.10 MB
english, 2019