Citations for
1ACSL4, MRX63, MRX68
X inactivation testing for identifying a non-syndromic X-linked mental retardation gene.
Yonath H, Marek-Yagel D, Resnik-Wolf H, Abu-Horvitz A, Baris HN, Shohat M, Frydman M, Pras E.
J Appl Genet Appl Genet. 2011 May 17. [Epub ahead of print] 2011
2ACSL4, MRX68, MRX63
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies.
Bhat SS, Schmidt KR, Ladd S, Kim KC, Schwartz CE, Simensen RJ, DuPont BR, Stevenson RE, Srivastava AK.
Cytogenet Genome Res 112(1-2):170-5. 2006
3MRX63
X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms.
Frints SG, Froyen G, Marynen P, Fryns JP.
Clin Genet 62(6):423-32. 2002