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NTNG1 mutations are a rare cause of Rett syndrome.

Pubmed ID: 
16502428
Year: 
2006
Month: 
Apr
Volume: 
140
Issue: 
7
Citation: 
Archer HL, Evans JC, Millar DS, Thompson PW, Kerr AM, Leonard H, Christodoulou J, Ravine D, Lazarou L, Grove L, Verity C, Whatley SD, Pilz DT, Sampson JR, Clarke AJ. NTNG1 mutations are a rare cause of Rett syndrome. American journal of medical genetics. Part A 140 (7) : 691 - 4(2006) PubMed