- Title: Subtitle
- Novel mutations seen in rapid, fatal case of early onset LAL deficiency (Wolman disease)
- Creators
- Mariana Gomez-Najera - Hospital de Ginecopediatria #48 IMSS, León, Guanajuato, MexicoHilario Barajas-Medina - Hospital de Ginecopediatria #48 IMSS, León, Guanajuato, MexicoMayra Celina Gallegos-Rivas - Hospital de Ginecopediatria #48 IMSS, León, Guanajuato, MexicoPedro Mendez-Sashida - Hospital de EspecialidadesAmy Simonds - Synageva BioPharmaRadhika Tripuraneni - Synageva BioPharmaYadira Valles-Ayoub - HIBM Research Group, Los Angeles, CA, USAYasemen Eroglu - Oregon Health & Science University
- Resource Type
- Abstract
- Publication Details
- Molecular genetics and metabolism, Vol.108(2), pp.S44-S45
- Publisher
- Elsevier Inc
- DOI
- 10.1016/j.ymgme.2012.11.100
- ISSN
- 1096-7192
- eISSN
- 1096-7206
- Language
- English
- Date published
- 02/2013
- Academic Unit
- Stead Family Department of Pediatrics; Gastroenterology, Hepatology, Pancreatology, and Nutrition
- Record Identifier
- 9984691524702771
Abstract
Novel mutations seen in rapid, fatal case of early onset LAL deficiency (Wolman disease)
Molecular genetics and metabolism, Vol.108(2), pp.S44-S45
02/2013
DOI: 10.1016/j.ymgme.2012.11.100
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