Open AccessA case of netherton syndrome with novel mutation in SPINK5 gene expressing incomplete phenotype
Author(s) -
Tejas D Patel,
Jignaben Krunal Padhiyar,
Nayan H Patel,
Nishi Trivedi
Publication year - 2020
Publication title -
indian journal of paediatric dermatology
Language(s) - English
Resource type - Journals
eISSN - 2319-7269
pISSN - 2319-7250
DOI - 10.4103/ijpd.ijpd_76_19
Subject(s) - medicine , phenotype , mutation , gene , gene mutation , genetics , biology