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Volumn 12, Issue 4, 2003, Pages 237-239

M Varallo: A New M Like Alpha 1-Antitrypsin-Deficient Allele

Author keywords

Alpha 1 antitryspin deficiency; Chronic airflow limitation; New M like variant

Indexed keywords

ALPHA 1 ANTITRYPSIN; BETA ADRENERGIC RECEPTOR STIMULATING AGENT; DNA; TRYPSIN INHIBITOR;

EID: 0344851808     PISSN: 10529551     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019606-200312000-00008     Document Type: Article
Times cited : (8)

References (12)
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    • Nukiwa, T.1    Satoh, K.2    Brantly, M.L.3
  • 3
    • 0021752456 scopus 로고
    • Complete sequence of the cDNA for human alpha-1-antitrypsin and the gene for the S variant
    • Long GL, Chandra T, Woo SL, et al. Complete sequence of the cDNA for human alpha-1-antitrypsin and the gene for the S variant. Biochemistry (Mosc). 1984;23:4828-4837.
    • (1984) Biochemistry (Mosc) , vol.23 , pp. 4828-4837
    • Long, G.L.1    Chandra, T.2    Woo, S.L.3
  • 6
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    • Siiyama (serine 53 (TCC) to phenylalanine 53 (TTC)). A new alpha 1-antitrypsin-deficient variant with mutation on a predicted conserved residue of the serpin backbone
    • Seyama K, Nukiwa T, Takabe K, et al. Siiyama (serine 53 (TCC) to phenylalanine 53 (TTC)). A new alpha 1-antitrypsin-deficient variant with mutation on a predicted conserved residue of the serpin backbone. J Biol Chem. 1991;266:12627-12632.
    • (1991) J Biol Chem , vol.266 , pp. 12627-12632
    • Seyama, K.1    Nukiwa, T.2    Takabe, K.3
  • 9
    • 0025193198 scopus 로고
    • Alpha-1-antitrypsin Null (Isola di Procida): An alpha-1-antitrypsin deficiency allele caused by deletion of alpha-1-antitrypsin coding exon
    • Takahashi H, Crystal RG. Alpha-1-antitrypsin Null (Isola di Procida): an alpha-1-antitrypsin deficiency allele caused by deletion of alpha-1-antitrypsin coding exon. Am J Hum Genet. 1990;47:403-413.
    • (1990) Am J Hum Genet , vol.47 , pp. 403-413
    • Takahashi, H.1    Crystal, R.G.2
  • 10
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    • Finnegan, D.J.1
  • 11
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    • Deficit di alfa-1-antitripsina. Descrizione di un caso clinico a fenotipo ZZ e con bronchiettasie come principale manifestazione clinica
    • Balbi B, Fiasella F, Fabiano F. Deficit di alfa-1-antitripsina. Descrizione di un caso clinico a fenotipo ZZ e con bronchiettasie come principale manifestazione clinica. Rassegna di Patologia dell' Apparato Respiratorio 1994;9:254-257.
    • (1994) Rassegna di Patologia dell' Apparato Respiratorio , vol.9 , pp. 254-257
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  • 12
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    • A national program for detection of alpha-1-antitrypsin deficiency in Italy
    • Luisetti M, Massi G, Massobrio M, et al. A national program for detection of alpha-1-antitrypsin deficiency in Italy. Resp. Med. 1999;93:169-172.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.