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

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Veröffentlicht in:	European journal of endocrinology 2019-12, Vol.181 (6), p.C29-C33
Hauptverfasser:	Walenkamp, M J E, Wit, J M
Format:	Artikel
Sprache:	eng
Schlagworte:	Commentary Growth Disorders - genetics Hearing Loss, Sensorineural - genetics Humans Insulin-like growth factor I Insulin-Like Growth Factor I - deficiency Insulin-Like Growth Factor I - genetics Mutation - genetics Tyrosine - genetics
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doi_str_mv	10.1530/EJE-19-0801
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source	MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects	Commentary Growth Disorders - genetics Hearing Loss, Sensorineural - genetics Humans Insulin-like growth factor I Insulin-Like Growth Factor I - deficiency Insulin-Like Growth Factor I - genetics Mutation - genetics Tyrosine - genetics
title	A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency
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