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Adult gaucher disease in southern Tunisia: report of three cases

BACKGROUND: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far the most common form. It is characterized by variability in age of onset, clinical signs and progression. It is usually diagnosed in the first or second decade of life with the appearance of bone pains...

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Detalhes bibliográficos
Main Authors: Ben Rhouma, Faten, Kallel, Faten, Kefi, Rym, Cherif, Wafa, Nagara, Majdi, Azaiez, Hela, Jedidi, Ines, Elloumi, Moez, Abdelhak, Sonia, Mseddi, Sondes
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3275535/
https://ncbi.nlm.nih.gov/pubmed/22233685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-1596-7-4
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