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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.

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Title: Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
Authors: Ferda Percin, E., Ploder, Lynda A., Yu, Jessica J., Arici, Kemal, Jonathan Horsford, D., Rutherford, Adam, Bapat, Bharati, Cox, Diane W., Duncan, Alessandra M.V., Kalnins, Vitauts I., Kocak-Altintas, Aysegul, Sowden, Jane C., Traboulsi, Elias, Sarfarazi, Mansoor, McInnes, Roderick R.
Source: Nature Genetics. Aug2000, Vol. 25 Issue 4, p397. 5p.
Database: Academic Search Ultimate
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  Data: Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
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  Data: <searchLink fieldCode="JN" term="%22Nature+Genetics%22">Nature Genetics</searchLink>. Aug2000, Vol. 25 Issue 4, p397. 5p.
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