Your browser doesn't support javascript.
loading
Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families.
Pashaei, Mahdieh; Davarzani, Atefeh; Hajati, Reza; Zamani, Babak; Nafissi, Shahriar; Larti, Farzaneh; Nilipour, Yalda; Rohani, Mohammad; Alavi, Afagh.
Affiliation
  • Pashaei M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Davarzani A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Hajati R; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Zamani B; Neurology Department, Firoozgar hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Nafissi S; Department of Neurology, Shariati Hospital., Tehran University of Medical Sciences, Tehran, Iran.
  • Larti F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Nilipour Y; Pediatric Pathology Research Center, Research Institute for Children Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Rohani M; Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
J Neurogenet ; 35(2): 84-94, 2021.
Article in En | MEDLINE | ID: mdl-33771085
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apyrase / Steroid Hydroxylases / Spastic Paraplegia, Hereditary / Carrier Proteins / Cytochrome P450 Family 7 Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: J Neurogenet Year: 2021 Type: Article Affiliation country: Iran
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apyrase / Steroid Hydroxylases / Spastic Paraplegia, Hereditary / Carrier Proteins / Cytochrome P450 Family 7 Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: J Neurogenet Year: 2021 Type: Article Affiliation country: Iran