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Volumn 7, Issue 2, 2000, Pages 121-125

Transthyretin isoleucine-122 mutation in African and American blacks

Author keywords

Amyloidosis; Cardiomyopathy; Hereditary; Isoleucine 122; Transthyretin

Indexed keywords

ISOLEUCINE; PREALBUMIN;

EID: 0034031238     PISSN: 13506129     EISSN: None     Source Type: Journal    
DOI: 10.3109/13506120009146249     Document Type: Article
Times cited : (12)

References (15)
  • 1
    • 0003490570 scopus 로고
    • Madison University of Wisconsin Press
    • Curtin P (1969). The Atlantic Slave. Madison University of Wisconsin Press
    • (1969) The Atlantic Slave
    • Curtin, P.1
  • 3
    • 44949277138 scopus 로고
    • Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (Ile-122)
    • Nichols WC, Liepnieks JJ, Synder EL, and Benson MD (1991). Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (Ile-122). J Lab Med 117, 175-180
    • (1991) J Lab Med , vol.117 , pp. 175-180
    • Nichols, W.C.1    Liepnieks, J.J.2    Synder, E.L.3    Benson, M.D.4
  • 5
    • 0025819856 scopus 로고
    • Frequency and genetic background of the position 122 (Val Ile) variant transthyretin gene in the Black population
    • Jacobson DR, Reveille JD and Buxbaum JN (1991). Frequency and genetic background of the position 122 (Val Ile) variant transthyretin gene in the Black population. Am J Hum Genet 49, 192-198
    • (1991) Am J Hum Genet , vol.49 , pp. 192-198
    • Jacobson, D.R.1    Reveille, J.D.2    Buxbaum, J.N.3
  • 6
    • 0026543251 scopus 로고
    • A homozygous transthyretin variant associated with senile amyloidosis: Evidence for a late-onset disease of genetic etiology
    • Jacobson DR, Gorevic PD, and Buxbaum JN (1992). A homozygous transthyretin variant associated with senile amyloidosis: evidence for a late-onset disease of genetic etiology. Am J Hum Genet 50, 195-198
    • (1992) Am J Hum Genet , vol.50 , pp. 195-198
    • Jacobson, D.R.1    Gorevic, P.D.2    Buxbaum, J.N.3
  • 9
    • 0001999309 scopus 로고
    • Amyloidosis
    • Scriver CR, Beaudet AK, Sly WS, Valle D (eds.). New York: McGraw-Hill
    • Benson, MD (1995). Amyloidosis. In Scriver CR, Beaudet AK, Sly WS, Valle D (eds.) The Metabolic and Molecular Bases of Inherited Disease, pp. 4159-4191. (New York: McGraw-Hill)
    • (1995) The Metabolic and Molecular Bases of Inherited Disease , pp. 4159-4191
    • Benson, M.D.1
  • 10
    • 0024560416 scopus 로고
    • Systemic senile amyloidosis - Identification of a new prealbumin (transthyretin) variant in cardiac tissue: Immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy
    • Gorevic PD, Prelli FC, Wright J, Pras M, and Frangione B (1989). Systemic senile amyloidosis - identification of a new prealbumin (transthyretin) variant in cardiac tissue: Immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy. J Clin Invest 83, 836-843
    • (1989) J Clin Invest , vol.83 , pp. 836-843
    • Gorevic, P.D.1    Prelli, F.C.2    Wright, J.3    Pras, M.4    Frangione, B.5
  • 14
    • 0024756969 scopus 로고
    • Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
    • Orita M, Suzuki Y, Sekiya T, and Hayashi P (1989). Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 5, 874-879
    • (1989) Genomics , vol.5 , pp. 874-879
    • Orita, M.1    Suzuki, Y.2    Sekiya, T.3    Hayashi, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.