A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: Differential role of the polyalanine tract in the development of the ovary and the eyelid

Kenjiro Kosaki, Tsutomu Ogata, Rika Kosaki, Seiji Sato, Nobutake Matsuo

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20 Citations (Scopus)

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Medicine & Life Sciences