AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis | Journal of Medical Genetics

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AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis

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Cite this article as:: Andreoletti G, Seaby EG, Dewing JM, et al

AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis

Journal of Medical Genetics 2017;54:269-277.