X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype

Detalles Bibliográficos
Autores principales:	Whyte, M, Christie, P, Podgornik, M, Dixon, P, Eddy, M, Wooding, C, Trump, D, Grieff, M, Mumm, S, Shlessinger, D, Thakker, R
Formato:	Journal article
Publicado:	1999

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