Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 6 (of 6 Records) |
Query Trace: Hyperprolinemia[original query] |
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PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Human molecular genetics 2002 Sep 11 (19): 2243-9. Jacquet Hélène, Raux Grégory, Thibaut Florence, Hecketsweiler Bernadette, Houy Emmanuelle, Demilly Caroline, Haouzir Sadeq, Allio Gabrielle, Fouldrin Gael, Drouin Valérie, Bou Jacqueline, Petit Michel, Campion Dominique, Frébourg Thier |
Functional consequences of PRODH missense mutations. American journal of human genetics 2005 1 76 (3): 409-20. Bender Hans-Ulrich, Almashanu Shlomo, Steel Gary, Hu Chien-An, Lin Wei-Wen, Willis Alecia, Pulver Ann, Valle Dav |
Hyperprolinemia is not associated with childhood onset schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006 1 141B (2): 192. Jacquet Hélène, Rapoport Judith L, Hecketsweiler Bernadette, Bobb Aaron, Thibaut Florence, Frébourg Thierry, Campion Dominiq |
Type I hyperprolinemia: genotype/phenotype correlations. Human mutation 2010 Aug 31 (8): 961-5. Guilmatre Audrey, Legallic Solenn, Steel Gary, Willis Alecia, Di Rosa Gabriella, Goldenberg Alice, Drouin-Garraud Valérie, Guet Agnès, Mignot Cyril, Des Portes Vincent, Valayannopoulos Vassili, Van Maldergem Lionel, Hoffman Jodi D, Izzi Claudia, Espil-Taris Caroline, Orcesi Simona, Bonafé Luisa, Le Galloudec Eric, Maurey Hélène, Ioos Christine, Afenjar Alexandra, Blanchet Patricia, Echenne Bernard, Roubertie Agathe, Frebourg Thierry, Valle David, Campion Dominiq |
PRODH rs450046 and proline x COMT Val¹58 Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome. Psychopharmacology 2015 Sep 232 (17): 3111-22. de Koning Mariken B, van Duin Esther D A, Boot Erik, Bloemen Oswald J N, Bakker Jaap A, Abel Kathryn M, van Amelsvoort Thérèse A M |
Psychiatric phenotypes associated with hyperprolinemia: A systematic review. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2021 7 186 (5): 289-317. Namavar Yasmin, Duineveld Denise Joanne, Both Geertje Ingena Angelique, Fiksinski Ania Maria, Vorstman Jacob Abraham Schrey, Verhoeven-Duif Nanda Margriet, Zinkstok Janneke Rozemari |
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- Page last updated:Apr 22, 2024
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