Uncovering the missing mutations in pain-Reference-Cited by-同舟云学术

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Uncovering the missing mutations in pain

Published:2024-05-07 Issue:9 Volume:165 Page:1901-1903
ISSN:0304-3959
Container-title:Pain
language:en
Short-container-title:Pain

Author:

Pham Quoc Thao Trang¹²^ORCID,Weng Hao-Jui¹³⁴⁵^ORCID

Affiliation:

1. International Ph.D. Program in Cell Therapy and Regenerative Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

2. Department of Dermatology, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam

3. Department of Dermatology, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan

4. Department of Dermatology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

5. Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan

Funder

National Science and Technology Council

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference17 articles.

1. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype;Altassan;Am J Med Genet A,2017

2. Structural and functional properties of the TRK family of neurotrophin receptors;Barbacid;Ann N Y Acad Sci,1995

3. Congenital insensitivity to pain and anhydrosis (CIPA) syndrome: a report of 4 cases;Daneshjou;Iran J Pediatr,2012

4. A case of congenital general pure analgesia;Dearborn;J Nervous Ment Dis,1932

5. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis;Indo;Nat Genet,1996

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