Tangier disease with syringomyelia-like phenotype in a family from Afghanistan caused by a novel mutation in the ABCA1 gene
Year: 2006
Type: article
Study design: Case Report
Source: Aktuelle Neurologie
Authors: S. Schippling, T. Rosenkranz, P. Vogel, U. Beisiegel, A. Münchau, C. Hagel, U. Seedorf
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2056424549
