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

M. J.E. Walenkamp, J. M. Wit^*

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Original language	English
Pages (from-to)	C29-C33
Journal	European Journal of Endocrinology
Volume	181
Issue number	6
DOIs	https://doi.org/10.1530/EJE-19-0801
Publication status	Published - 1 Jan 2019

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title = "A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency",

author = "Walenkamp, {M. J.E.} and Wit, {J. M.}",

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AU - Walenkamp, M. J.E.

AU - Wit, J. M.

PY - 2019/1/1

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M3 - Comment/Letter to the editor

C2 - 31614333

AN - SCOPUS:85076524973

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SP - C29-C33

JO - European Journal of Endocrinology

JF - European Journal of Endocrinology

SN - 0804-4643

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