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A novel gain-of-function mutation (F821L) in the transmembrane domain of calcium-sensing receptor is a cause of severe sporadic hypoparathyroidism

✍ Scribed by Masaaki Shiohara; Tetsuo Mori; Bai Mei; EdwardM. Brown; Tomoyuki Watanabe; Toshiyuki Yasuda

Publisher: Springer
Year: 2004
Tongue: English
Weight: 269 KB
Volume: 163
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00431-003-1331-7

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