A NOVEL ASPARTYLGLUCOSAMINURIA MUTATION IN A PATIENT WITH CO-EXISTENCE OF GAUCHER DISEASE

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Bibliographic Details
Published in:	Genetic counseling Vol. 26; no. 4; p. 463
Main Authors:	Kiykim, E, Zubarioglu, T, Gorukmez, O, Gunes, S, Cansever, M S, Zeybek, A C Aktuglu
Format:	Journal Article
Language:	English
Published:	Switzerland 01-01-2015
Subjects:	Aspartylglucosaminuria - complications Aspartylglucosaminuria - genetics Child, Preschool Gaucher Disease - complications Gaucher Disease - genetics Humans Male Mutation Polymorphism, Restriction Fragment Length - genetics
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ISSN:	1015-8146