A novel A178P mutation in SLC16A2...

Congenital Anomalies 2017 / 09

A novel A178P mutation in SLC16A2 in a patient with Allan-Herndon-Dudley syndrome

Yamamoto, Toshiyuki, Lu, Yongping, Nakamura, Ryoko, Shimojima, Keiko, Kira, Ryutaro
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Language:
english
Journal:
Congenital Anomalies
DOI:
10.1111/cga.12251
Date:
September, 2017
File:
PDF, 991 KB
english, 2017
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