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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
Philippe Jay
Claire Rougeulle
1
Annick Massacrier
Anne Moncla
Marie-Geneviève Mattel
Perrine Malzac
Nathalie Roëckel
Sylvie Taviaux
Jean-Louis Bergé Lefranc
Pierre Cau
Philippe Berta
Marc Lalande
Françoise Muscatelli
Philippe Jay
Author IdHAL : philippe-jay ResearcherId : http://www.researcherid.com/rid/I-7116-2016 IdRef : https://www.idref.fr/120996049 ORCID : https://orcid.org/0000-0003-0156-5700
Claire Rougeulle 1
Author
Annick Massacrier
Author
Anne Moncla
Author
Françoise Muscatelli
Author
1
EDC (UMR_7216) - Centre épigénétique et destin cellulaire (Université Paris Diderot Bât. Lamarck case postale 7042 75205 Paris CEDEX 13 - France)
- CNRS - Centre National de la Recherche Scientifique : UMR_7216 (France)
- UP - Université de Paris : UMR_7216 (85 boulevard Saint-Germain 75006 Paris - France)
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Journal articles
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https://hal-cnrs.archives-ouvertes.fr/hal-03030605
Contributor : Mathieu Manquant Connect in order to contact the contributor
Submitted on : Monday, November 30, 2020 - 10:50:13 AM
Last modification on : Tuesday, September 28, 2021 - 5:15:44 PM
Contributor : Mathieu Manquant Connect in order to contact the contributor
Submitted on : Monday, November 30, 2020 - 10:50:13 AM
Last modification on : Tuesday, September 28, 2021 - 5:15:44 PM
Identifiers
- HAL Id : hal-03030605, version 1
- DOI : 10.1038/ng1197-357
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Citation
Philippe Jay, Claire Rougeulle, Annick Massacrier, Anne Moncla, Marie-Geneviève Mattel, et al.. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics, Nature Publishing Group, 1997, 17 (3), pp.357-361. ⟨10.1038/ng1197-357⟩. ⟨hal-03030605⟩
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