Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pai...
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain
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Author / Creator
Kantaputra, Piranit , Daroontum, Teerada , Kitiyamas, Kantapong , Piyakhunakorn, Panat , Kawasaki, Katsushige , Sathienkijkanchai, Achara , Wasant, Pornswan , Vatanavicharn, Nithiwat , Yasanga, Thippawan , Kaewgahya, Massupa , Tongsima, Sissades , Cox, Timothy C. , Arold, Stefan T. , Ohazama, Atsushi and Ngamphiw, Chumpol
Publisher
Switzerland: MDPI AG
Journal title
Language
English
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Publication information
Publisher
Switzerland: MDPI AG
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Scope and Contents
Contents
Congenital insensitivity to pain is a rare human condition in which affected individuals do not experience pain throughout their lives. This study aimed to identify the molecular etiology of congenital insensitivity to pain in two Thai patients. Clinical, radiographic, histopathologic, immunohistochemical, and molecular studies were performed. Pati...
Alternative Titles
Full title
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11203604
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11203604
Other Identifiers
ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms25126358
