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Academic Journal

Clinical and molecular characteristics of Wiskott-Aldrich Syndrome in five unrelated Chinese families.

  • Authors : Jiang J; Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.; Zhou J

Subjects: Leukocytes, Mononuclear/Leukocytes, Mononuclear/Leukocytes, Mononuclear/*metabolism ; Mutation/Mutation/Mutation/*genetics ; Wiskott-Aldrich Syndrome/Wiskott-Aldrich Syndrome/Wiskott-Aldrich Syndrome/*immunology

  • Source: Scandinavian journal of immunology [Scand J Immunol] 2022 Jan; Vol. 95 (1), pp. e13115. Date of Electronic Publication: 2021 Nov 16.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 0323767 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.

  • Authors : Liu DW; Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital, Chongqing Medical University, Chongqing, China.; Zhang ZY

Subjects: Mutation*; Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/*genetics ; Thrombocytopenia/Thrombocytopenia/Thrombocytopenia/*genetics Thrombocytopenia 1

  • Source: Pediatric blood & cancer [Pediatr Blood Cancer] 2015 Sep; Vol. 62 (9), pp. 1601-8. Date of Electronic Publication: 2015 Apr 30.Publisher: John Wiley Country of Publication: United States NLM ID: 101186624 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.

Subjects: Mutation, Missense*; Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/*genetics ; Thrombocytopenia/Thrombocytopenia/Thrombocytopenia/*genetics Thrombocytopenia 1

  • Source: Clinical laboratory [Clin Lab] 2018 Oct 31; Vol. 64 (11).Publisher: Clinical Laboratory Publications Country of Publication: Germany NLM ID: 9705611 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.

Subjects: ESSENTIAL tremor; GENETIC variation; GENE expressionCHINA

  • Source: Neurological Sciences; Jun2023, Vol. 44 Issue 6, p2003-2015, 13p, 1 Black and White Photograph, 1 Diagram, 2 Charts, 1 Graph

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  • 1-10 of  40 results for ""Wiskott-Aldrich Syndrome Protein""