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ALX4 null mutations underlie alopecia

Posted by ArnaudMartin on 05 Mar 2017 at 19:26 GMT

This additional reference maybe relevant to the identification of ALX4 as a MBP candidate gene.
Kayserili et al. Hum Mol Genet 2009 "ALX4 dysfunction disrupts craniofacial and epidermal development " https://doi.org/10.1093/h...

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