Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma - Paulina

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Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma

journal article; published in Acta Oto-Laryngologica Case Reports in 2017

Author/s

author: Shin-Ichi Usami

Work details

Publication date

January 2017

Language

English

Copyright status

copyrighted