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Homozygous Missense Variants in NTNG2, Encoding a Presynapt..:
Dias, Caroline M.
;
Punetha, Jaya
;
Zheng, Céline
...
The American Journal of Human Genetics. 105 (2019) 5 - p. 1048-1056 , 2019
Link:
https://doi.org/10.1016/j.ajhg.2019.09.025
RT Journal T1
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2019.09.025&Exemplar=1&LAN=DE A1 Dias, Caroline M. A1 Punetha, Jaya A1 Zheng, Céline A1 Mazaheri, Neda A1 Rad, Abolfazl A1 Efthymiou, Stephanie A1 Petersen, Andrea A1 Dehghani, Mohammadreza A1 Pehlivan, Davut A1 Partlow, Jennifer N. A1 Posey, Jennifer E. A1 Salpietro, Vincenzo A1 Gezdirici, Alper A1 Malamiri, Reza Azizi A1 Al Menabawy, Nihal M. A1 Selim, Laila A. A1 Vahidi Mehrjardi, Mohammad Yahya A1 Banu, Selina A1 Polla, Daniel L. A1 Yang, Edward A1 Rezazadeh Varaghchi, Jamileh A1 Mitani, Tadahiro A1 van Beusekom, Ellen A1 Najafi, Maryam A1 Sedaghat, Alireza A1 Keller-Ramey, Jennifer A1 Durham, Leslie A1 Coban-Akdemir, Zeynep A1 Karaca, Ender A1 Orlova, Valeria PB Elsevier BV YR 2019 SN 0002-9297 JF The American Journal of Human Genetics VO 105 IS 5 SP 1048 OP 1056 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2019.09.025 DO https://doi.org/10.1016/j.ajhg.2019.09.025 SF ELIB - SuUB Bremen
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