Publications by authors named "Christian Gund"

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Identification of a syndrome comprising microcephaly and intellectual disability but not white matter disease associated with a homozygous c.676C>T p.R226W DEAF1 mutation.
Christian Gund, Zöe Powis, Wendy Alcaraz, Sonal Desai, Kristin Baranano

Am J Med Genet A· May 2016

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