A single nucleotide deletion resulting in a frameshift in exon 4 of TAB2 is associated with a polyvalular syndrome
Permanyer, Eduard, Laurie, Steven, Blasco-Lucas, Arnau, Maldonado, Giuliana, Amador-Catalan, Amaya, Ferrer-Curriu, Gemma, Fuste, Berta, Perez, Maria L., Gonzalez-Alujas, Teresa, Beltran, Sergi, Comas-Riu, Jaume, Bardají, Alfredo, Evangelista, Artur, Galiñanes, Manuel
Published in European journal of medical genetics (01.04.2020)
Published in European journal of medical genetics (01.04.2020)
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