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	1.	Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutations. [electronic resource] by Hume, Alistair N John, Anne Akawi, Nadia A Al-Awadhi, Aydah M Al-Suwaidi, Sarah S Al-Gazali, Lihadh Ali, Bassam R Producer: 20130531 In: Molecular and cellular biochemistry vol. 373 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Defective cellular trafficking of missense NPR-B mutants is the major mechanism underlying acromesomelic dysplasia-type Maroteaux. [electronic resource] by Hume, Alistair N Buttgereit, Jens Al-Awadhi, Aydah M Al-Suwaidi, Sarah S John, Anne Bader, Michael Seabra, Miguel C Al-Gazali, Lihadh Ali, Bassam R Producer: 20090203 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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