The H723R mutation in the PDS/SLC26A4 gene is associated with typical pendred syndrome in korean patients

Author: Cho Mi   Jeong Su   Eom Sang-Mi   Park Hyun-Yung   Lee Young   Park Se   Park So   Rhee Yumie   Kang Eun   Ahn Chul   Cha Bong   Lee Eun   Kim Kyung   Lee Hyun   Lim Sung-Kil  

Publisher: Humana Press, Inc

ISSN: 0969-711X

Source: Endocrine Journal, Vol.30, Iss.2, 2006-10, pp. : 237-243

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