Identification of a novel homozygous frameshift mutation in SLC29A3 gene in a case with H syndrome from Iran.
Bagherian R, Yousefipour F, Mousavi HS, Saffari F, HajiShafieha E, Mohammadi SN, Mousakhani H, Fathi SM, Mehrtash A, Verki FM, Lee D, Heidari A.
Bagherian R, et al. Among authors: mousavi hs.
Curr Res Transl Med. 2019 May;67(2):72-75. doi: 10.1016/j.retram.2019.01.003. Epub 2019 Feb 2.
Curr Res Transl Med. 2019.
PMID: 30723056