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Article

Novel A178P mutation in SLC16A2 in a patient with Allan-Herndon-Dudley syndrome.

Congenital anomalies - 1 Jul 2018

Yamamoto Toshiyuki, Lu Yongping, Nakamura Ryoko, Shimojima Keiko, Kira Ryutaro

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PMID: 28862359
DOI: 10.1111/cga.12251

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