Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients

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Abstract

In a recent association study carried out in US patients with autism spectrum disorder (ASD), Ingram et al (2000) reported detection of linkage between ASD and a mutation of HOXA1, a homeotic gene playing a role in early brain formation. In contrast, in an attempt to replicate these findings, the authors found a negative association between polymorphisms of the HOXA1 and HOXB1 genes and autism in 85 Sicilian (Italian) families.

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Romano, V., Calí, F., Mirisola, M., Gambino, G., D’ Anna, R., Di Rosa, P., … Elia, M. (2003). Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients. Molecular Psychiatry, 8(8), 716-717+713. https://doi.org/10.1038/sj.mp.4001285

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