Molecular analysis of acid ceramidase deficiency in patients with Farber disease-Reference-Cited by-同舟云学术

Molecular analysis of acid ceramidase deficiency in patients with Farber disease

Published:2001-02-23 Issue:3 Volume:17 Page:199-209
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bär Julia,Linke Thomas,Ferlinz Klaus,Neumann Ulrich,Schuchman Edward H.,Sandhoff Konrad

Funder

Fortüne-program of University of Tübingen

Graduiertenkolleg “Functional protein domains”

Deutsche Forschungsgemeinschaft

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference37 articles.

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5. A simple method for screening for Farber disease on cultured skin fibroblasts;Chatelut;Clin Chim Acta,1996

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