The E37X is a common HMGCL mutation in Portuguese patients...

Molecular Genetics and Metabolism 2004 Vol. 82; Iss. 4

The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiency

M.L Cardoso, M.R Rodrigues, E Leão, E Martins, L Diogo, E Rodrigues, P Garcia, M.O Rolland, L Vilarinho
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Volume:
82
Year:
2004
Language:
english
DOI:
10.1016/j.ymgme.2004.06.003
File:
PDF, 828 KB
english, 2004
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