Splice Site Mutations in GH1 Detected in Previously (Genetically) Undiagnosed Families with Congenital Isolated Growth Hormone Deficiency Type II

Author(s):
Kempers, M.J.E.; Crabben, S.N. van der; Vroede, M. de; Alfen-van der Velden, J.; Netea-Maier, R.T.; Duim, R.A.J.; Otten, B.J.; Losekoot, M.; Wit, J.M.
Published
2013
Publication type
Article / Letter to editor
Congenital isolated growth hormone deficiencyGH1 geneSplice site mutationsGrowth hormone
Date issued
2013-12-31
Language
English
Is part of
Hormone Research in Paediatrics (2013), Vol. 80, no. 6, p. 390-396
hdl
1887/99875
doi
10.1159/000355403