A novel IGSF1 mutation in a large Irish kindred highlights the need for systematic familial endocrine screening in the IGSF1 deficiency syndrome

作者:McGowan A; Roche E; Koulouri O; Turgeon M O; Nicholas A K; Heffernan E; El Khairi R; Lyons G; Persani L; Dattani M T; Gurnell M; Bernard D J; Schoenmakers N
  • 出版日期2017-9