Identification of the Peroxisomal Biogenesis Factor 1 Gene Point Mutation in an Iranian Family with Zellweger Syndrome (ZS) | Zendy

Negin Parsamanesh | Zendy; Azam Ahmadi Shadmehri | Zendy; Shahnaz Zarifi | Zendy; Ebrahim MiriMoghaddam | Zendy

Open Access

Identification of the Peroxisomal Biogenesis Factor 1 Gene Point Mutation in an Iranian Family with Zellweger Syndrome (ZS)

Author(s) -

Negin Parsamanesh,

Azam Ahmadi Shadmehri,

Shahnaz Zarifi,

Ebrahim MiriMoghaddam

Publication year - 2021

Publication title -

journal of advances in medical and biomedical research

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.113

H-Index - 12

ISSN - 2676-6264

DOI - 10.30699/jambs.29.134.167

Subject(s) - zellweger syndrome , biogenesis , peroxisomal disorder , point mutation , identification (biology) , peroxisome , mutation , gene , genetics , biology , botany

1. Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran 2. Student Research Committee, Birjand University of Medical Sciences, Birjand, Iran 3. Social Welfare Organization of South Khorasan Province, Birjand, Iran 4. Cardiovascular Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran 5. Dept. of Molecular Medicine, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran

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