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Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.
Sawal, H A; Harripaul, R; Mikhailov, A; Dad, R; Ayub, M; Jawad Hassan, M; Vincent, J B.
Affiliation
  • Sawal HA; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Harripaul R; Atta-ur-Rahman School of Applied Biosciences, National University of Sciences and Technology (NUST), Islamabad, Pakistan.
  • Mikhailov A; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Dad R; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Ayub M; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Jawad Hassan M; Atta-ur-Rahman School of Applied Biosciences, National University of Sciences and Technology (NUST), Islamabad, Pakistan.
  • Vincent JB; Department of Psychiatry, Queen's University, Kingston, ON, Canada.
Clin Genet ; 90(6): 563-565, 2016 12.
Article in En | MEDLINE | ID: mdl-27747863
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pain Insensitivity, Congenital / NAV1.7 Voltage-Gated Sodium Channel / Mutation Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2016 Document type: Article Affiliation country: Canada Country of publication: Denmark
Fulltext
Add to My VHL
Print
XML
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pain Insensitivity, Congenital / NAV1.7 Voltage-Gated Sodium Channel / Mutation Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2016 Document type: Article Affiliation country: Canada Country of publication: Denmark