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

---

Autoria(s): Superti-Furga A.; Steinmann B.; Duc G.; Gitzelmann R.

Data(s)	1990
Identificador	http://serval.unil.ch/?id=serval:BIB_B631B052AD6A isbn:0031-3998 isiid:A1990DV86100107
Idioma(s)	en
Fonte	Annual Meeting of the European Society for Pediatric Research
Tipo	info:eu-repo/semantics/conferenceObject inproceedings