Literature citations
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.
Narumi S.; Amano N.; Ishii T.; Katsumata N.; Muroya K.; Adachi M.; Toyoshima K.; Tanaka Y.; Fukuzawa R.; Miyako K.; Kinjo S.; Ohga S.; Ihara K.; Inoue H.; Kinjo T.; Hara T.; Kohno M.; Yamada S.; Urano H.; Kitagawa Y.; Tsugawa K.; Higa A.; Miyawaki M.; Okutani T.; Kizaki Z.; Hamada H.; Kihara M.; Shiga K.; Yamaguchi T.; Kenmochi M.; Kitajima H.; Fukami M.; Shimizu A.; Kudoh J.; Shibata S.; Okano H.; Miyake N.; Matsumoto N.; Hasegawa T.;
Nat. Genet. 48:792-797(2016)
Cited for: INVOLVEMENT IN MIRAGE; VARIANTS MIRAGE GLN-459; ASN-769; TYR-834; LYS-974; VAL-1195; LEU-1280; LYS-1286 AND TRP-1293; CHARACTERIZATION OF VARIANTS MIRAGE GLN-459; ASN-769; TYR-834; LYS-974; VAL-1195; LEU-1280; LYS-1286 AND TRP-1293;
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