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Volumn 104, Issue 8, 2004, Pages 2607-

Molecular characterization of a third case of human atransferrinemia [1]

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFERRIN;

EID: 19544369489     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2004-05-1751     Document Type: Letter
Times cited : (36)

References (12)
  • 2
    • 0015543930 scopus 로고
    • Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia
    • Stavem P, Saltvedt E, Elgjo K, Rootwelt K. Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia. Scand J Haematol. 1973;10:153-160.
    • (1973) Scand J Haematol , vol.10 , pp. 153-160
    • Stavem, P.1    Saltvedt, E.2    Elgjo, K.3    Rootwelt, K.4
  • 4
    • 0031612929 scopus 로고    scopus 로고
    • Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group
    • Antonarakis SE. Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group. Hum Mutat. 1998;11:1-3.
    • (1998) Hum Mutat , vol.11 , pp. 1-3
    • Antonarakis, S.E.1
  • 5
    • 0033987736 scopus 로고    scopus 로고
    • Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
    • den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000;15:7-12.
    • (2000) Hum Mutat , vol.15 , pp. 7-12
    • Den Dunnen, J.T.1    Antonarakis, S.E.2
  • 6
    • 0015384214 scopus 로고
    • A family of congenital atransferrinemia
    • Goya N, Miyazaki S, Kodate S, Ushio B. A family of congenital atransferrinemia. Blood. 1972;40:239-245.
    • (1972) Blood , vol.40 , pp. 239-245
    • Goya, N.1    Miyazaki, S.2    Kodate, S.3    Ushio, B.4
  • 7
    • 0027360042 scopus 로고
    • Studies on familial hypotransferrinemia: Unique clinical course and molecular pathology
    • Hayashi A, Wada Y, Suzuki T, Shimizu A. Studies on familial hypotransferrinemia: unique clinical course and molecular pathology. Am J Hum Genet. 1993; 53:201-213.
    • (1993) Am J Hum Genet , vol.53 , pp. 201-213
    • Hayashi, A.1    Wada, Y.2    Suzuki, T.3    Shimizu, A.4
  • 8
    • 0036308217 scopus 로고    scopus 로고
    • Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia
    • Asada-Senju M, Maeda T, Sakata T, Hayashi A, Suzuki T. Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia. J Hum Genet. 2002;47:355-359.
    • (2002) J Hum Genet , vol.47 , pp. 355-359
    • Asada-Senju, M.1    Maeda, T.2    Sakata, T.3    Hayashi, A.4    Suzuki, T.5
  • 9
    • 0014340744 scopus 로고
    • Kongenitálna atransferinémia u 11-mesačného diet'at'a
    • Čáp J, Lehotská V, Mayerová A. Kongenitálna atransferinémia u 11-mesačného diet'at'a. Cesk Pediatr. 1968;23:1020-1025.
    • (1968) Cesk Pediatr , vol.23 , pp. 1020-1025
    • Čáp, J.1    Lehotská, V.2    Mayerová, A.3
  • 11
    • 4944225586 scopus 로고
    • Kongenitale atransferrinämie: Klinische beobachtungen während einer 18jährigen substitution mit humantransferrin
    • Hromec A, Čáp J, Schwick HG. Kongenitale Atransferrinämie: Klinische Beobachtungen während einer 18jährigen Substitution mit Humantransferrin. Pädiatr Praxis. 1989;38:633-637.
    • (1989) Pädiatr Praxis , vol.38 , pp. 633-637
    • Hromec, A.1    Čáp, J.2    Schwick, H.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.