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	1.	CITRIN DEFICIENCY: AN INFANT INCIDENTALLY DETECTED BY PHENYLKETONURIA SCREENING WITH A NOVEL MUTATION IN SLC25A13 GENE. [electronic resource] by Zeybek, A C Aktuglu Kiykim, E Zubarioglu, T Cansever, M S Ceylaner, S Erkan, T Producer: 20160303 In: Genetic counseling (Geneva, Switzerland) vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	2.	A NOVEL ASPARTYLGLUCOSAMINURIA MUTATION IN A PATIENT WITH CO-EXISTENCE OF GAUCHER DISEASE. [electronic resource] by Kiykim, E Zubarioglu, T Gorukmez, O Gunes, S Cansever, M S Zeybek, A C Aktuglu Producer: 20160303 In: Genetic counseling (Geneva, Switzerland) vol. 26 Availability: No items available. Save to lists Add to cart (remove)

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