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Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Zweier, Markus, Gogoll, Laura, Schiffmann, Raphael, Sticht, Heinrich
ORCID: https://orcid.org/0000-0001-5644-045X, Steindl, Katharina and Rauch, Anita
(2017)
Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation.
European Journal of Medical Genetics, 60 (9).
pp. 451-464.
ISSN 1769-7212
(doi:10.1016/j.ejmg.2017.06.004)