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Volumn 77, Issue 2, 2010, Pages 189-192

Identities and frequencies of BMPR2 mutations in Chinese patients with idiopathic pulmonary arterial hypertension

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN RECEPTOR 2; GENOMIC DNA;

EID: 73949145107     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2009.01335.x     Document Type: Letter
Times cited : (9)

References (13)
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  • 2
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  • 3
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    • Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
    • The International PPH Consortium
    • Lane KB, Machado RD, Pauciulo MW. Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension. Nat Genet 2000, 26:81-84. The International PPH Consortium
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  • 4
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    • Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
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  • 5
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  • 6
    • 66249125359 scopus 로고    scopus 로고
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  • 7
    • 32544438253 scopus 로고    scopus 로고
    • BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension
    • Aldred MA, Vijayakrishnan J, James V. BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension. Hum Mutat 2006, 27:212-213.
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  • 8
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  • 9
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  • 13
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.