Author:
Suzuki Yoshiro,Chitayat David,Sawada Hirotake,Deardorff Matthew A.,McLaughlin Heather M.,Begtrup Amber,Millar Kathryn,Harrington Jennifer,Chong Karen,Roifman Maian,Grand Katheryn,Tominaga Makoto,Takada Fumio,Shuster Shirley,Obara Megumi,Mutoh Hiroshi,Kushima Reiko,Nishimura Gen
Funder
Ministry of Education, Culture, Sports, Science, and Technology
Subject
Genetics (clinical),Genetics
Reference37 articles.
1. Bone metabolism during pregnancy;Salles;Ann. Endocrinol. (Paris),2016
2. Mutations in SPATA5 are associated with microcephaly, intellectual disability, seizures, and hearing loss;Tanaka;Am. J. Hum. Genet.,2015
3. Structural conservation of the genes encoding CaT1, CaT2, and related cation channels;Peng;Genomics,2001
4. The in vivo TRPV6 protein starts at a non-AUG triplet, decoded as methionine, upstream of canonical initiation at AUG;Fecher-Trost;J. Biol. Chem.,2013
5. Parallel selection on TRPV6 in human populations;Hughes;PLoS ONE,2008
Cited by
51 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献