Author:
Barboura Ilhem,Hadded Samir,Chebel Saber,Mansour Rachida Ben,Chahed Hinda,Gueddiche Mohamed-Néji,Frih-Ayed Mahbouba,Ferchichi Salima,Miled Abdelhédi
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Reference13 articles.
1. Von Figura K, Gieselmann V, Jaeken J: Metachromatic leukodystrophy. The Metabolic and Molecular Bases of Inherited Disease. Edited by: Scriver CR, Beaudet AL, Sly WS, Valle D. 2001, New York:McGraw-Hill, 3695-3724.
2. Önder E, Sinici I, Sönmez FM, Topçu M, Özkara HA: Identification of two novel arylsulfatase A mutation with a polymorphism as a cause of metachromatic leukodystrophy. Neurological Research. 2009, 31: 60-66. 10.1179/016164108X323762.
3. Austin JH, Armstrong D, Sheara I, McAfee D: Metachromatic form of diffuse cerebral sclerosis VI. A rapid test for the sulfatase A deficiency in metachromatic leukodystrophy (MLD) urine. Arch Neurol. 1966, 14: 259-10.1001/archneur.1966.00470090031004.
4. Lowry OH, Rosebrough NJ, Farr AL, et al.: Protein measurement with folin phenol reagent. J Biol Chem. 1951, 193: 265-275.
5. Suzuki K: Enzymatic diagnosis of sphingolipidoses. Methods enzymol. 1987, 138: 727-763.
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献