Home > A. Molecular pathology > NKX5-3
NKX5-3
Friday 25 April 2008
Pathology
germline mutations of NKX5-3 in oculo-auricular syndrome (18423520).
References
Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL. Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome. Am J Hum Genet. 2008 Apr 16; PMID: 18423520
