✦ LIBER ✦

Association of the Hermansky–Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects

✍ Scribed by Kuratomi, Go; Saito, Atsushi; Ozeki, Yuji; Watanabe, Takashi; Fujii, Kumiko; Shimoda, Kazutaka; Inukai, Toshihiko; Mori, Harunobu; Ohmori, Kenichi; Akiyama, Kazufumi

Book ID: 121605761
Publisher: BioMed Central
Year: 2013
Tongue: English
Weight: 247 KB
Volume: 13
Category: Article
ISSN: 1471-244X
DOI: 10.1186/1471-244X-13-276

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Association of genetic variations in DTN

Association of genetic variations in DTNBP1 with cognitive function in schizophrenia patients and healthy subjects

✍ Ji Hyun Baek; Ji Sun Kim; Seunghyong Ryu; Sohee Oh; Jihae Noh; Woo Kyeong Lee; T 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 128 KB

Interaction of dopamine system genes and

Interaction of dopamine system genes and cognitive functions in patients with schizophrenia and their relatives and in healthy subjects from the general population

✍ M. V. Alfimova; V. E. Golimbet; I. K. Gritsenko; T. V. Lezheiko; L. I. Abramova; 📂 Article 📅 2007 🏛 Springer US 🌐 English ⚖ 125 KB

Poster #102 THE ASSOCIATION OF NRG1, DTN

Poster #102 THE ASSOCIATION OF NRG1, DTNBP1, RGS4, G72/G30, DISCI AND BDNF CANDIDATE GENES WITH COGNITION IN PATIENTS WITH SCHIZOPHRENIA AND HEALTHY CONTROLS

✍ János M. Réthelyi; Patricia Polgár; Judit Benkovits; Kinga Farkas; Attila J. Pul 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 66 KB

P02-215 - The association of NRG1, DTNBP

P02-215 - The association of NRG1, DTNBP1, RGS4, G72/G30 and PIP5K2A candidate genes with cognition in patients with schizophrenia and healthy controls

✍ J.M. Réthelyi; P. Polgár; J. Benkovits; É. Jekkel; P. Czobor; I. Bitter 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 12 KB

Deletion of the first pair of fibronecti

Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients

✍ Ramon Y. Birnbaum; Daniella Landau; Khalil Elbedour; Rivka Ofir; Ohad S. Birk; R 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 147 KB 👁 1 views

Deletion of the first pair of fibronectin type III repeats of the integrin b-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients.