Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
Faridi, R., Rehman, A.U., Morell, R.J., Friedman, P.L., Demain, L., Zahra, S., Khan, A.A., Tohlob, D., Assir, M.Z., Beaman, G., Khan, S.N., Newman, W.G., Riazuddin, S., Friedman, T.B.
Published in Clinical genetics (01.02.2017)
Published in Clinical genetics (01.02.2017)
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