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	1.	Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX gene. [electronic resource] by Zou, Minjing Buluş, Derya Al-Rijjal, Roua A Andıran, Nesibe BinEssa, Huda Kattan, Walaa E Meyer, Brian Shi, Yufei Producer: 20150922 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Acylpeptide hydrolase is a novel regulator of KRAS plasma membrane localization and function. [electronic resource] by Tan, Lingxiao Cho, Kwang-Jin Kattan, Walaa E Garrido, Christian M Zhou, Yong Neupane, Pratik Capon, Robert J Hancock, John F Producer: 20200709 In: Journal of cell science vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Targeting plasma membrane phosphatidylserine content to inhibit oncogenic KRAS function. [electronic resource] by Kattan, Walaa E Chen, Wei Ma, Xiaoping Lan, Tien Hung van der Hoeven, Dharini van der Hoeven, Ransome Hancock, John F Producer: 20200629 In: Life science alliance vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A. [electronic resource] by Demir, Korcan Kattan, Walaa E Zou, Minjing Durmaz, Erdem BinEssa, Huda Nalbantoğlu, Özlem Al-Rijjal, Roua A Meyer, Brian Özkan, Behzat Shi, Yufei Producer: 20160425 In: PloS one vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets. [electronic resource] by Guven, Ayla Al-Rijjal, Roua A BinEssa, Huda A Dogan, Durmuş Kor, Yılmaz Zou, Minjing Kaya, Namik Alenezi, Anwar F Hancili, Suna Tarım, Ömer Baitei, Essa Y Kattan, Walaa E Meyer, Brian F Shi, Yufei Producer: 20180319 In: Clinical endocrinology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis. [electronic resource] by Zou, Minjing Alzahrani, Ali S Al-Odaib, Ali Alqahtani, Mohammad A Babiker, Omer Al-Rijjal, Roua A BinEssa, Huda A Kattan, Walaa E Al-Enezi, Anwar F Al Qarni, Ali Al-Faham, Manar S A Baitei, Essa Y Alsagheir, Afaf Meyer, Brian F Shi, Yufei Producer: 20181211 In: The Journal of clinical endocrinology and metabolism vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3. [electronic resource] by Acar, Sezer BinEssa, Huda A Demir, Korcan Al-Rijjal, Roua A Zou, Minjing Çatli, Gönül Anık, Ahmet Al-Enezi, Anwar F Özışık, Seçil Al-Faham, Manar S A Abacı, Ayhan Dündar, Bumin Kattan, Walaa E Alsagob, Maysoon Kavukçu, Salih Tamimi, Hamdi E Meyer, Brian F Böber, Ece Shi, Yufei Producer: 20180702 In: PloS one vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)