(Q51912838)
Statements
Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patient. (English)
1 reference
Akira Miyauchi
1 reference
Eijun Nishihara
1 reference
Shuji Fukata
1 reference
Akira Hishinuma
1 reference
Takumi Kudo
1 reference
Hidemi Ohye
1 reference
Mitsuru Ito
1 reference
Sumihisa Kubota
1 reference
Nobuyuki Amino
1 reference
Kanji Kuma
1 reference
7 September 2006
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53
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6
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735-740
1 reference