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Article

Hereditary Sensory Polyneuropathy, Pain Insensitivity and Global Developmental Delay due to Novel Mutation in PRDM12 Gene.

Indian journal of pediatrics - 1 Apr 2017

Saini Arushi Gahlot, Padmanabh Hansashree, Sahu Jitendra Kumar, Kurth Ingo, Voigt Martin, Singhi Pratibha

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Identifiers

PMID: 28050684
DOI: 10.1007/s12098-016-2284-y

Genes

PRDM12

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Hereditary Sensory Polyneuropathy, Pain Insensitivity and Global Developmental Delay due to Novel Mutation in PRDM12 Gene.PMID 28050684Read ↗

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Clinical and electrophysiologic features of the Pediatric hereditary neuropathy with liability to pressure palsiesSemantic proximity Read ↗

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Prdm12 Directs Nociceptive Sensory Neuron Development by Regulating the Expression of the NGF Receptor TrkASemantic proximity Read ↗

Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.Semantic proximity Read ↗

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