论文信息 - Two novel CLN5 mutations in a Portuguese patient with vLINCL: insights into molecular mechanisms of CLN5 deficiency. - 字舞流文

Two novel CLN5 mutations in a Portuguese patient with vLINCL: insights into molecular mechanisms of CLN5 deficiency.

J. Ferreira | P. Cabral | A. Guimarães | M. S. Sá Miranda | C. Bessa | M. G. Ribeiro | C. Teixeira | M. Mangas | A. Dias | N. Canas