A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency

Author(s):
Walenkamp, M.J.E.; Wit, J.M.
Published
2019
Publication type
Article / Letter to editor
Date issued
2019-12-31
Language
English
Is part of
European Journal of Endocrinology (2019), Vol. 181, no. 6, p. C29-C33
hdl
1887/3195451
doi
10.1530/EJE-19-0801