Search Results - "Volozonoka, L."

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders by Oud, M S, Houston, B J, Volozonoka, L, Mastrorosa, F K, Holt, G S, Alobaidi, B K S, deVries, P F, Astuti, G, Ramos, L, Mclachlan, R I, O'Bryan, M K, Veltman, J A, Chemes, H E, Sheth, H

“…What are the causative genetic variants in patients with male infertility due to severe sperm motility disorders? We identified high confidence disease-causing…”
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Lack of evidence for a role of PIWIL1 variants in human male infertility by Oud, M.S., Volozonoka, L., Friedrich, C., Kliesch, S., Nagirnaja, L., Gilissen, C., O’Bryan, M.K., McLachlan, R.I., Aston, K.I., Tüttelmann, F., Conrad, D.F., Veltman, J.A.

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