Maternal PKU syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase-261 ARG-]GLN mutation.

Details

Serval ID
serval:BIB_B631B052AD6A
Type
Inproceedings: an article in a conference proceedings.
Publication sub-type
Abstract (Abstract): shot summary in a article that contain essentials elements presented during a scientific conference, lecture or from a poster.
Collection
Publications
Institution
Title
Maternal PKU syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase-261 ARG-]GLN mutation.
Title of the conference
Annual Meeting of the European Society for Pediatric Research
Author(s)
Superti-Furga A., Steinmann B., Duc G., Gitzelmann R.
Address
Vienna, Austria, September 23-27, 1990
ISBN
0031-3998
Publication state
Published
Issued date
1990
Peer-reviewed
Oui
Volume
28
Series
Pediatric Research
Pages
291
Language
english
Web of science
Create date
14/03/2011 16:14
Last modification date
20/08/2019 15:24
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