Open AccessA Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome)
Author(s) -
Elise Schaefer Maryline Minoux
Publication year - 2014
Publication title -
journal of genetic syndromes and gene therapy
Language(s) - English
Resource type - Journals
ISSN - 2157-7412
DOI - 10.4172/2157-7412.1000251
Subject(s) - microtia , agenesis , medicine , mutation , anatomy , biology , bioinformatics , surgery , genetics , gene
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