Predicting the impact of PHEX, FGF23 and DMP1 gene variants found in Malaysian Malay patients with Hypophosphataemic Rickets through in silico analysis of protein function and mRNA secondary structure

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Predicting the impact of PHEX, FGF23 and DMP1 gene variants found in Malaysian Malay patients with Hypophosphataemic Rickets through in silico analysis of protein function and mRNA secondary structure

Hypophosphataemic Rickets (HR) is a rare bone disorder characterised by chronic hypophosphataemia caused by defective phosphate reabsorption in the renal tubules. Variants in phosphate-regulating endopeptidase homolog, X-linked (PHEX), fibroblast growth factor-23 (...

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Bibliographic Details
Main Authors:	Razali, Nurul Nadirah, Hwu, Ting Tzer, King, Hwa Ling, Marina, L. Kennerson, Thilakavathy, Karuppiah
Format:	Article
Language:	English
Published:	Hibiscus Publisher 2019
Online Access:	http://psasir.upm.edu.my/id/eprint/81783/ http://psasir.upm.edu.my/id/eprint/81783/1/Predicting%20the%20impact%20of%20PHEX.pdf

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