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A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy.
Naderi, Niloofar; Mohsen-Pour, Neda; Nilipour, Yalda; Pourirahim, Maryam; Maleki, Majid; Kalayinia, Samira.
Afiliación
  • Naderi N; Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, University of Medical Sciences, Tehran, Iran.
  • Mohsen-Pour N; Zanjan Pharmaceutical Biotechnology Research Center, Zanjan University of Medical Sciences, Zanjan, Iran.
  • Nilipour Y; Pediatric pathology research center, Research institute for children's health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Pourirahim M; Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, University of Medical Sciences, Tehran, Iran.
  • Maleki M; Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, University of Medical Sciences, Tehran, Iran.
  • Kalayinia S; Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, University of Medical Sciences, Tehran, Iran. samira.kalayi@yahoo.com.
BMC Cardiovasc Disord ; 23(1): 487, 2023 10 04.
Article en En | MEDLINE | ID: mdl-37794383
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cardiomiopatía Dilatada / Enfermedades Musculares Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Child / Humans País/Región como asunto: Asia Idioma: En Revista: BMC Cardiovasc Disord Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Irán
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cardiomiopatía Dilatada / Enfermedades Musculares Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Child / Humans País/Región como asunto: Asia Idioma: En Revista: BMC Cardiovasc Disord Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Irán