Jinks, R. N., Puffenberger, E. G., Baple, E., Harding, B., Crino, P., Fogo, A. B., . . . Strauss, K. A. (2015). Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. Brain.
Styl cytowania ChicagoJinks, Robert N., et al. "Recessive Nephrocerebellar Syndrome On the Galloway-Mowat Syndrome Spectrum Is Caused By Homozygous Protein-truncating Mutations of WDR73." Brain 2015.
Styl cytowania MLAJinks, Robert N., et al. "Recessive Nephrocerebellar Syndrome On the Galloway-Mowat Syndrome Spectrum Is Caused By Homozygous Protein-truncating Mutations of WDR73." Brain 2015.
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