Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
par Raux, Grégory;Bumsel, Emilie;Hecketsweiler, Bernadette;van Amelsvoort, Therese;Zinkstok, Janneke;Manouvrier-Hanu, Sylvie;Fantini-Hauwel, Carole 
;Brévière, Georges-Marie M;Di Rosa, Gabriella;Pustorino, Giuseppina;Vogels, Annick;Swillen, Ann;Legallic, Solenn;Bou, Jacqueline;Opolczynski, Gaelle;Drouin-Garraud, Valérie;Lemarchand, Marie;Philip, Nicole;Gérard-Desplanches, Aude;Carlier, Michèle;Philippe, Anne;Nolen, Marie Christine;Heron, Delphine;Sarda, Pierre;Lacombe, Didier;Coizet, Cyril;Alembik, Yves;Layet, Valérie;Afenjar, Alexandra;Hannequin, Didier;Demily, Caroline;Petit, Michel ;Thibaut, Florence;Frebourg, Thierry;Campion, Dominique
Référence Human molecular genetics, 16, 1, page (83-91)
Publication Publié, 2007
;Brévière, Georges-Marie M;Di Rosa, Gabriella;Pustorino, Giuseppina;Vogels, Annick;Swillen, Ann;Legallic, Solenn;Bou, Jacqueline;Opolczynski, Gaelle;Drouin-Garraud, Valérie;Lemarchand, Marie;Philip, Nicole;Gérard-Desplanches, Aude;Carlier, Michèle;Philippe, Anne;Nolen, Marie Christine;Heron, Delphine;Sarda, Pierre;Lacombe, Didier;Coizet, Cyril;Alembik, Yves;Layet, Valérie;Afenjar, Alexandra;Hannequin, Didier;Demily, Caroline;Petit, Michel ;Thibaut, Florence;Frebourg, Thierry;Campion, DominiqueRéférence Human molecular genetics, 16, 1, page (83-91)
Publication Publié, 2007
Article révisé par les pairs
| Titre: |
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| Auteur: | Raux, Grégory; Bumsel, Emilie; Hecketsweiler, Bernadette; van Amelsvoort, Therese; Zinkstok, Janneke; Manouvrier-Hanu, Sylvie; Fantini-Hauwel, Carole; Brévière, Georges-Marie M; Di Rosa, Gabriella; Pustorino, Giuseppina; Vogels, Annick; Swillen, Ann; Legallic, Solenn; Bou, Jacqueline; Opolczynski, Gaelle; Drouin-Garraud, Valérie; Lemarchand, Marie; Philip, Nicole; Gérard-Desplanches, Aude; Carlier, Michèle; Philippe, Anne; Nolen, Marie Christine; Heron, Delphine; Sarda, Pierre; Lacombe, Didier; Coizet, Cyril; Alembik, Yves; Layet, Valérie; Afenjar, Alexandra; Hannequin, Didier; Demily, Caroline; Petit, Michel; Thibaut, Florence; Frebourg, Thierry; Campion, Dominique |
| Informations sur la publication: | Human molecular genetics, 16, 1, page (83-91) |
| Statut de publication: | Publié, 2007 |
| Sujet CREF: | Physiopsychologie et psychologie biologique [psychiatrie] |
| Sciences humaines | |
| MeSH keywords: | Adolescent |
| Adult | |
| Alleles | |
| Catechol O-Methyltransferase -- genetics | |
| Chromosome Deletion | |
| Chromosomes, Human, Pair 22 -- genetics | |
| DiGeorge Syndrome -- genetics -- psychology | |
| Epilepsy -- blood -- enzymology -- genetics | |
| Female | |
| Genetic Predisposition to Disease | |
| Humans | |
| Intellectual Disability -- blood -- enzymology -- genetics | |
| Male | |
| Methionine -- genetics | |
| Middle Aged | |
| Phenotype | |
| Proline -- blood -- genetics | |
| Proline Oxidase -- genetics | |
| Psychotic Disorders -- blood -- enzymology -- genetics | |
| Risk Factors | |
| Note générale: | Journal Article |
| Research Support, Non-U.S. Gov't | |
| Langue: | Anglais |
| Identificateurs: | urn:issn:0964-6906 |
| info:doi/10.1093/hmg/ddl443 | |
| info:pii/ddl443 | |
| info:pmid/17135275 |
