Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome;: no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome
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作者:
Ki, CS
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Ki, CS
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Jin, DK
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Jin, DK
[1
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Chang, SH
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Chang, SH
[1
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Kim, JE
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Kim, JE
[1
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Kim, JW
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Kim, JW
[1
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Park, BK
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Park, BK
[1
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Choi, JH
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Choi, JH
[1
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Park, IS
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Park, IS
[1
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Yoo, HW
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Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South KoreaSungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
Yoo, HW
[1
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机构:
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
机构:
Fu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
PUMC, Beijing 100037, Peoples R ChinaFu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
Zhang, Lin
Zhou, Xianliang
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Fu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
PUMC, Beijing 100037, Peoples R ChinaFu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
Zhou, Xianliang
Gao, Linggen
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Fu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
PUMC, Beijing 100037, Peoples R ChinaFu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
Gao, Linggen
Hui, Rutai
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机构:
Cardiovasc Inst, Div Hypertens, Beijing 100037, Peoples R China
Key Lab Clin Cardiovasc Genet, Beijing 100037, Peoples R China
Sino German Lab Mol Med, Beijing 100037, Peoples R ChinaFu Wai Hosp, CAMS, Div Hypertens, Beijing 100037, Peoples R China
机构:
Univ Zurich, Inst Med Genet, Div Med Mol Genet & Gene Diagnost, Zurich, SwitzerlandKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
Henggeler, C.
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Wierzba, J.
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Loeys, B.
De Paepe, A.
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机构:
Ghent Univ Hosp, Ctr Med Genet, B-9000 Ghent, BelgiumKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
De Paepe, A.
Stheneur, Ch.
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机构:
Hop Ambroise Pare, AP HP, Serv Pediat, Boulogne, France
Hop Bichat Claude Bernard, AP HP, F-75877 Paris, FranceKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
Stheneur, Ch.
Badziag, N.
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机构:
Karol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, PolandKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
Badziag, N.
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Matuszewska, K.
Matyas, G.
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机构:
Univ Zurich, Inst Med Genet, Div Med Mol Genet & Gene Diagnost, Zurich, SwitzerlandKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
Matyas, G.
Latos-Bielenska, A.
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机构:
Karol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland
Ctr Med Genet Poznan, Poznan, PolandKarol Marcinkowski Univ Med Sci, Dept Med Genet, PL-60352 Poznan, Poland