Open AccessA novel mutation of CAPN1 gene causing hereditary spastic Paraplegia-76
Author(s) -
VijayendraR 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 , mutation , paraplegia , spastic , gene mutation , genetics , gene , physical medicine and rehabilitation , biology , phenotype , cerebral palsy , spinal cord , psychiatry