The novel p.Ser263Phe mutation in the human high‐affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndrome
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Stacey Hume | O. Caluseriu | N. Leonard | M. Banerjee | J. Watt | E. Leslie | D. Arutyunov | A. Lacson | Daniel Brandwein | H. Kolski | Emmanuelle Cordat | Cassandra Janetzki-Flatt | Monica Baradi