Novel A178P mutation in SLC16A2 in a patient with Allan ‐Herndon‐Dudley syndrome
Source: Congenital Anomalies - Category: Genetics & Stem Cells Authors: Toshiyuki Yamamoto, Yongping Lu, Ryoko Nakamura, Keiko Shimojima, Ryutaro Kira Tags: Note Source Type: research
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