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Updated: Aug 11, 2025

12:49
Mutagenesis and Analysis of Genetic Mutations in the GC-rich KISS1 Receptor Sequence Identified in Humans with Reproductive Disorders
Published on: September 4, 2011
14.0K
A novel KRT14 null mutation leads to autosomal recessive epidermolysis bullosa simplex
Lauren Banner1, Alexa Cohen1, Lauren McGrath1
1Department of Dermatology and Cutaneous Biology, Philadelphia, PA, USA.
Clinical and Experimental Dermatology
|February 9, 2023
Abstract
No abstract available in PubMed .
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