Open AccessA Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
Author(s) -
VijayendraReddy Chinta,
Pramod Krishnan
Publication year - 2022
Publication title -
annals of indian academy of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_977_21
Subject(s) - medicine , hereditary spastic paraplegia , spasticity , weakness , phenocopy , proband , spastic , locus (genetics) , paraplegia , physical medicine and rehabilitation , pediatrics , genetics , mutation , anatomy , phenotype , gene , spinal cord , biology , psychiatry , cerebral palsy
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