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- W3035288549 abstract "<br>Lack of pain sensation in children involves a rare group of heritable disorders; hereditary sensory and autonomic neuropathy (HSAN). Till date, eight types of HSAN have been described depending on the clinical phenotype and the underlying gene mutation. We report a new variant of HSAN (Type IX) in two siblings (of Indian origin) with a novel mutation of <i>SCN11A</i>gene and a distinct clinical phenotype.<br>" @default.
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- W3035288549 date "2020-01-01" @default.
- W3035288549 modified "2023-09-27" @default.
- W3035288549 title "Sisters with no pain, no tears: A report of a new variant of hereditary sensory and autonomic neuropathy (Type IX) Caused by a novel SCN11A mutation" @default.
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- W3035288549 doi "https://doi.org/10.4103/ijd.ijd_416_18" @default.
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