Open AccessGRISCELLI SYNDROME TYPE 2: THE FIRST REPORTED CASE OF COMPOUND HETEROZYGOUS MUTATION IN RAB 27 A GENE FROM INDIA
Author(s) -
Nishad Dhakate,
Manjit Rajput
Publication year - 2019
Publication title -
indian journal of case reports
Language(s) - English
Resource type - Journals
eISSN - 2454-1303
pISSN - 2454-129X
DOI - 10.32677/ijcr.2019.v05.i06.002
Subject(s) - medicine , compound heterozygosity , mutation , genetics , rab , gene , biology , gtpase
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