12881_2019_908_Fig6_HTML.png,The Epilepsy–Aphasia Syndrome Gene, Cnksr2, Plays a Critical,Identification of a HOXD13 variant in a Mongolian family,A nonsense mutation in the HOXD13 gene underlies,A heterozygous duplication variant of the HOXD13 gene caused激レア。【新品・未開封】Taylor Swift Lover ラヴァー 限定盤。UK盤 ACTIVE CDATV17#thrash