RT Journal Article
SR Electronic
T1 Mutations in exon 1 of <em>MECP2</em> are a rare cause of Rett syndrome
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP e15
OP e15
DO 10.1136/jmg.2004.026161
VO 42
IS 2
A1 Amir, R E
A1 Fang, P
A1 Yu, Z
A1 Glaze, D G
A1 Percy, A K
A1 Zoghbi, H Y
A1 Roa, B B
A1 Van den Veyver, I B
YR 2005
UL http://jmg.bmj.com/content/42/2/e15.abstract
AB