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Diagnostic dilemmas in Fabry disease: a case series study on GLA mutations of unknown clinical significance
Smid, B.E., Hollak, C.E.M., Poorthuis, B.J.H.M., van den Bergh Weerman, M.A., Florquin, S., Kok, W.E.M., Lekanne Deprez, R.H., Timmermans, J., Linthorst, G.E.Volume:
88
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12449
Date:
August, 2015
File:
PDF, 1.04 MB
english, 2015