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	1.	Novel mutations in the SMPD1 gene in Jordanian children with Acid sphingomyelinase deficiency (Niemann-Pick types A and B). [electronic resource] by Al-Eitan, Laith Alqa'qa', Kifah Amayreh, Wajdi Aljamal, Hanan Khasawneh, Rame Al-Zoubi, Batool Okour, Israa Haddad, Amany Haddad, Yazan Haddad, Hazem Producer: 20200518 In: Gene vol. 747 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification and Characterization of BTD Gene Mutations in Jordanian Children with Biotinidase Deficiency. [electronic resource] by Al-Eitan, Laith N Alqa'qa', Kifah Amayreh, Wajdi Khasawneh, Rame Aljamal, Hanan Al-Abed, Mamoon Haddad, Yazan Rawashdeh, Tamara Jaradat, Zaher Haddad, Hazem Publication details: Journal of personalized medicine Jan 2020 In: Journal of personalized medicine vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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