Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 (Q22337290)
scientific article
Language:
(P31) (Q13442814)
(P50) (Q1633764)
(Q54326298)
(P304) 185-188
(P407) (Q1860)
(P433) 2
(P478) 23
(P577) Friday, October 1, 1999
(P921) (Q917357)
(Q18028997)
(P1433) (Q976454)
(P1476) "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2" (language: en)
(P2093) Ruthie E. Amir
Ignatia B. Van den Veyver
Mimi Wan
Charles Q. Tran
(P2860) (Q48490930)
(Q34056069)
(Q39545733)
(Q41230681)
(Q35249570)
(Q43217591)
(Q41134121)
(Q72209605)
(Q43217978)
(Q24324026)
(Q29547568)
(Q38356105)
(Q28265233)
(Q24615012)
(Q28576622)
(Q52202965)
(Q42603699)
(Q22003967)
(Q22003762)
(Q36647235)
other details
description scientific article

External Links