Low prevalence of CHEK2 gene mutations in multiethnic cohorts of breast cancer patients in Malaysia.

Mohamad, Suriati; Isa, Nurismah Md; Muhammad, Rohaizak; Emran, Nor Aina; Kitan, Nor Mayah; Kang, Peter; Kang, In Nee; Taib, Nur Aishah Mohd; Teo, Soo Hwang; Akmal, Sharifah Noor

Mohamad, Suriati; Isa, Nurismah Md; Muhammad, Rohaizak; Emran, Nor Aina; Kitan, Nor Mayah; Kang, Peter; Kang, In Nee; Taib, Nur Aishah Mohd; Teo, Soo Hwang; Akmal, Sharifah Noor.

Afiliação

Mohamad S; Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Kuala Lumpur, Malaysia.
Isa NM; Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Kuala Lumpur, Malaysia.
Muhammad R; Department of Surgery, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Kuala Lumpur, Malaysia.
Emran NA; Department of General Surgery, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.
Kitan NM; Department of Endocrine Surgery, Hospital Putrajaya, Putrajaya, Malaysia.
Kang P; Cancer Research Initiative Foundation (CARIF), Subang Jaya, Selangor, Malaysia.
Kang IN; Cancer Research Initiative Foundation (CARIF), Subang Jaya, Selangor, Malaysia.
Taib NA; University Malaya Cancer Research Institute, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
Teo SH; Cancer Research Initiative Foundation (CARIF), Subang Jaya, Selangor, Malaysia; University Malaya Cancer Research Institute, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
Akmal SN; Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Kuala Lumpur, Malaysia.

PLoS One ; 10(1): e0117104, 2015.

Article em En | MEDLINE | ID: mdl-25629968

Assuntos

Neoplasias da Mama/genética; Quinase do Ponto de Checagem 2/genética; Predisposição Genética para Doença; Mutação de Sentido Incorreto; Adulto; Povo Asiático/genética; Neoplasias da Mama/etnologia; Neoplasias da Mama/patologia; Estudos de Casos e Controles; Feminino; Humanos; Malásia; Pessoa de Meia-Idade

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Quinase do Ponto de Checagem 2 Tipo de estudo: Observational_studies / Prevalence_studies Limite: Adult / Female / Humans / Middle aged País/Região como assunto: Asia Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Malásia

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