作者
J. Jeruzelska,Dominique Melle,Renata Matuszak,Krzysztof Borski,A Munnich
摘要
Journal Article A new 15 bp deletion in exon 11 of the phenylalanine hydroxylase gene in phenylketonuria Get access Jadwiga Jeruzelska, Jadwiga Jeruzelska * 1Institute of Human Genetics, Polish Academy of Sciencesul. Strzeszynska 32, 60-479 Poznan, Poland2Unité de Recherches sur les Handicaps Génétiques de I'EnfantINSERMU-12, Hospital des Enfants Malades, 149, rue de Sèvres, 75743 Paris cedex 15, France * To whom correspondence should be addressed at: Unité de Recherches sur les Handicaps Génétiques de I'Enfant, INSERM U-12, Hospital des Enfants Matades, 149, rue de Sèvres, 75743 Paris cedex 15, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Dominique Melle, Dominique Melle 2Unité de Recherches sur les Handicaps Génétiques de I'EnfantINSERMU-12, Hospital des Enfants Malades, 149, rue de Sèvres, 75743 Paris cedex 15, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Renata Matuszak, Renata Matuszak 1Institute of Human Genetics, Polish Academy of Sciencesul. Strzeszynska 32, 60-479 Poznan, Poland Search for other works by this author on: Oxford Academic PubMed Google Scholar Krzysztof Borski, Krzysztof Borski 3Institute of Pediatrics, Medical Academyul. Szpitalna 27/33, 60-572 Poznan, Poland Search for other works by this author on: Oxford Academic PubMed Google Scholar Arnold Munnich Arnold Munnich 2Unité de Recherches sur les Handicaps Génétiques de I'EnfantINSERMU-12, Hospital des Enfants Malades, 149, rue de Sèvres, 75743 Paris cedex 15, France Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 1, Issue 9, December 1992, Pages 763–764, https://doi.org/10.1093/hmg/1.9.763 Published: 01 December 1992 Article history Received: 23 October 1992 Accepted: 26 October 1992 Published: 01 December 1992