(Q35447613)
Statements
1 reference
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome (English)
1 reference
R E Amir
1 reference
P Fang
1 reference
Z Yu
1 reference
D G Glaze
1 reference
A K Percy
1 reference
B B Roa
1 reference
I B Van den Veyver
1 reference
1 February 2005
1 reference
1 reference
42
1 reference
2
1 reference
e15
1 reference
Identifiers
1 reference
1 reference
1 reference