Vol 2, No 1 (2018)

Case report
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 gene in child from Russia
Kulikova K.S., Vasiliev E.V., Petrov V.M., Tiulpakov A.N.
World Journal of Personalized Medicine. 2018;2(1):5-9
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(Rus)

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