Two novel mutations in the MECP2 gene in patients with Rett syndrome.

Autor:	Khalili Alashti, Shayan1 (AUTHOR) shayan.khalilii@gmail.com, Fallahi, Jafar2 (AUTHOR), Mohammadi, Sanaz3 (AUTHOR), Dehghanian, Fatemeh3 (AUTHOR), Farbood, Zahra3 (AUTHOR), Masoudi, Marjan3 (AUTHOR), Poorang, Shiva3 (AUTHOR), Jokar, Arezoo4 (AUTHOR), Fardaei, Majid1,3 (AUTHOR) mfardaei@sums.ac.ir
Zdroj:	Gene. Mar2020, Vol. 732, pN.PAG-N.PAG. 1p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu Full Text from ScienceDirect