Clinodactyly - A clinical clue to diagnose a hereditary periodic paralysis

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Published in:Annals of the Indian Academy of Neurology 2020-09, Vol.23 (5), p.738-739
Main Authors: Parihar, Jasmine, Vishnu, Venugopalan, Singh, Mamta, Goyal, Vinay, Padma Srivastava, M
Format: Article
Language:English
Subjects:
Abnormalities
Bones
Case studies
Diagnosis
Familial periodic paralysis
Letters to the Editor
Paralysis
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container_issue 5
container_start_page 738
container_title Annals of the Indian Academy of Neurology
container_volume 23
creator Parihar, Jasmine
Vishnu, Venugopalan
Singh, Mamta
Goyal, Vinay
Padma Srivastava, M
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doi_str_mv 10.4103/aian.AIAN_400_20
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ispartof Annals of the Indian Academy of Neurology, 2020-09, Vol.23 (5), p.738-739
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source PubMed Central (Open Access); Publicly Available Content Database; Medknow Medical Journals (Open access)
subjects Abnormalities
Bones
Case studies
Diagnosis
Familial periodic paralysis
Letters to the Editor
Paralysis
title Clinodactyly - A clinical clue to diagnose a hereditary periodic paralysis
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