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Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26.
Ullah, Anwar; Lin, Zhaohan; Younus, Muhammad; Shafiq, Sarfraz; Khan, Shazia; Rasheed, Memoona; Mahmood, Arif; Alqosaibi, Amany I; Alshehri, Mohammed Ali; Khan, Amjad; Umair, Muhammad.
Afiliación
  • Ullah A; Khyber Medical University Institute of Paramedical Science, Peshawar, Khyber Pakhtunkhwa, Pakistan.
  • Lin Z; State Key Laboratory of Membrane Biology and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine and Peking-Tsinghua Center for Life Sciences and PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing, China.
  • Younus M; State Key Laboratory of Membrane Biology and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine and Peking-Tsinghua Center for Life Sciences and PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing, China.
  • Shafiq S; Department of Anatomy and Cell Biology, Western University, London, ON, Canada.
  • Khan S; Department of Biological Sciences, International Islamic University Islamabad, Islamabad, Pakistan.
  • Rasheed M; Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, Pakistan.
  • Mahmood A; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Hunan, Changsha, China.
  • Alqosaibi AI; Institute of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Alshehri MA; Department of Biology, College of Science, Imam Abdulrahman bin Faisal University, Dammam, Saudi Arabia.
  • Khan A; Medical Genetics Laboratory Science, College of Applied medical Sciences, Najran University, Najran, Saudi Arabia.
  • Umair M; Faculty of Science, Department of Biological Sciences, University of Lakki Marwat, Lakki Marwat, Pakistan.
J Gene Med ; 24(4): e3412, 2022 04.
Article en En | MEDLINE | ID: mdl-35075722
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Distrofia Muscular de Cinturas / Proteínas Musculares Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: J Gene Med Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Pakistán
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Distrofia Muscular de Cinturas / Proteínas Musculares Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: J Gene Med Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Pakistán