Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene

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Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene

Author: Alves, Mariana Q.; Le Trionnaire, Emmanuelle; Ribeiro, Isaura; Carpentier, Stephane; Harzer, Klaus; Levade, Thierry; Gil Ribeiro, M.
Tübinger Autor(en):
Harzer, Klaus
Published in: Molecular Genetics and Metabolism (2013), Bd. 109, H. 3, S. 276-281
Verlagsangabe: Academic Press Inc Elsevier Science
Language: English
Full text: http://dx.doi.org/10.1016/j.ymgme.2013.04.019
ISSN: 1096-7192
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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