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Volumn 55, Issue 12, 2014, Pages 2945-2946

A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies

Author keywords

[No Author keywords available]

Indexed keywords

THROMBOPOIETIN; TRANSCRIPTION FACTOR GATA 2; TRANSCRIPTION FACTOR RUNX1; ANKRD26 PROTEIN, HUMAN; NUCLEAR PROTEIN;

EID: 84907987357     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.3109/10428194.2014.903476     Document Type: Letter
Times cited : (27)

References (7)
  • 2
    • 78650879044 scopus 로고    scopus 로고
    • Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2
    • Pippucci T, Savoia A, Perrotta S, et al. Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2. Am J Hum Genet 2011; 88: 115-120.
    • (2011) Am J Hum Genet , vol.88 , pp. 115-120
    • Pippucci, T.1    Savoia, A.2    Perrotta, S.3
  • 3
    • 79959279291 scopus 로고    scopus 로고
    • Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: Analysis of 78 patients from 21 families
    • Noris P, Perrotta S, Seri M, et al. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood 2011; 117: 6673-6680.
    • (2011) Blood , vol.117 , pp. 6673-6680
    • Noris, P.1    Perrotta, S.2    Seri, M.3
  • 4
    • 84884617225 scopus 로고    scopus 로고
    • A missense mutation in ANKRD26 segregates with thrombocytopenia
    • Al Daama SA, Housawi YH, Dridi W, et al. A missense mutation in ANKRD26 segregates with thrombocytopenia. Blood 2013; 122: 461-462.
    • (2013) Blood , vol.122 , pp. 461-462
    • Al Daama, S.A.1    Housawi, Y.H.2    Dridi, W.3
  • 5
    • 84887332514 scopus 로고    scopus 로고
    • ANKRD26-related thrombocytopenia and myeloid malignancies
    • Noris P, Favier R, Alessi MC, et al. ANKRD26-related thrombocytopenia and myeloid malignancies. Blood 2013; 122: 1987-1989.
    • (2013) Blood , vol.122 , pp. 1987-1989
    • Noris, P.1    Favier, R.2    Alessi, M.C.3
  • 6
    • 77956492055 scopus 로고    scopus 로고
    • A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5) identif ed in autosomal dominant thrombocytopenia
    • Punzo F, Mientjes EJ, Rohe CF, et al. A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5) identif ed in autosomal dominant thrombocytopenia. J Thromb Haemost 2010; 8: 2085-2087.
    • (2010) J Thromb Haemost , vol.8 , pp. 2085-2087
    • Punzo, F.1    Mientjes, E.J.2    Rohe, C.F.3
  • 7
    • 84870938434 scopus 로고    scopus 로고
    • Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes
    • Churpek JE, Lorenz R, Nedumgottil S, et al. Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes. Leuk Lymphoma 2013; 54: 28-35.
    • (2013) Leuk Lymphoma , vol.54 , pp. 28-35
    • Churpek, J.E.1    Lorenz, R.2    Nedumgottil, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.