Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome.
CLINICAL DYSMORPHOLOGY(2018)
Abstract
Atli, Engina; Gurkan, Hakana; Ulusal, Selmaa; Karal, Yaseminb; Atli, Emine I.a; Tozkir, Hilmia Author Information
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Human Inborn Errors
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