Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
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M. Vidailhet | A. Durr | M. Polak | D. Devos | L. Guillot | D. Rodriguez | R. Epaud | J. Koht | A. Camuzat | C. Goizet | J. Motte | E. Roze | M. Louha | T. Billette de Villemeur | S. Chantot-Bastaraud | B. Héron | D. Sanlaville | P. Charles | D. Doummar | M. Moutard | M. Tallot | I. Kemlin | L. Jonard | I. Vuillaume | D. Gras | I. Caubel | L. Lion‐François | B. Héron | L. Lion-François