Detection of adrenoleukodystrophy by increased C26:0 fatty acid levels in leukocytes
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
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5. Kombination von Morbus Addison und Morbus Schilder bei einer 43-jährigen Frau;Pilz;Acta Neuropathol (Berl),1973
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1. X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype;Biochemical and Biophysical Research Communications;2008-12
2. Diagnosis of X-linked adrenoleukodystrophy in blood leukocytes;Clinical Biochemistry;2007-09
3. Mutational Analysis of X-Linked Adrenoleukodystrophy Gene;Cell Biochemistry and Biophysics;2000
4. Mutational Analysis and Genotype-Phenotype Correlation of 29 Unrelated Japanese Patients With X-linked Adrenoleukodystrophy;Archives of Neurology;1999-03-01
5. X-linked adrenoleukodystrophy is a frequent cause of idiopathic Addison's disease in young adult male patients;Journal of Clinical Endocrinology & Metabolism;1996-02-01
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