Search Results - Assir, M.Z.

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    Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome

    Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome by 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
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