PMC Links for OMIM (Select 608458) - PMC - NCBI

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Select item 80593331.

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

Ambrin Fatima, Jan Hoeber, Jens Schuster, Eriko Koshimizu, Carolina Maya-Gonzalez, Boris Keren, Cyril Mignot, Talia Akram, Zafar Ali, Satoko Miyatake, Junpei Tanigawa, Takayoshi Koike, Mitsuhiro Kato, Yoshiko Murakami, Uzma Abdullah, Muhammad Akhtar Ali, Rein Fadoul, Loora Laan, Casimiro Castillejo-López, Maarika Liik, Zhe Jin, Bryndis Birnir, Naomichi Matsumoto, Shahid M. Baig, Joakim Klar, Niklas Dahl

Am J Hum Genet. 2021 Apr 1; 108(4): 739–748. Published online 2021 Mar 11. doi: 10.1016/j.ajhg.2021.02.015

Correction in:: Am J Hum Genet. 2022 Mar 3; 109(3): 542–546.

PMCID:: PMC8059333

Article PDF–1.9M

Select item 27965502.

Norbin is an endogenous regulator of metabotropic glutamate receptor 5 signaling

Hong Wang, Linda Westin, Yi Nong, Shari Birnbaum, Jacob Bendor, Hjalmar Brismar, Eric Nestler, Anita Aperia, Marc Flajolet, Paul Greengard

Science. Author manuscript; available in PMC 2009 Dec 21.

Published in final edited form as: Science. 2009 Dec 11; 326(5959): 1554–1557. doi: 10.1126/science.1178496

PMCID:: PMC2796550

Article PDF–432K

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