X-linked Adrenoleukodystrophy Mutations
Edit Page
Report
Scan day: 20 February 2014 UTC
8
Virus safety - good
Description: This database has been initiated to collect data on mutations found in the gene (ABCD1) responsible for X-linked adrenoleukodystrophy.
X-linked Adrenoleukodystrophy database X-linked Adrenoleukodystrophy Database X-linked adrenoleukodystrophy (X-ALD) is the most frequent inherited disorder of the central nervous system white matter with a minimum incidence of 1 in 17.000 newborns. It is a progressive, systemic metabolic disease that affects myelin, spinal cord, peripheral nerves, adrenal cortex and testis. The disease is caused by mutations in the
Size: 418 chars
Contact Information
Email: —
Phone&Fax: —
Address: —
Extended: —
WEBSITE Info
| Page title: | X-linked Adrenoleukodystrophy database |
| Keywords: | adrenoleukodystrophy, adrenomyeloneuropathy, adrenoleucodistrofia, adrénoleucodystrophie, adrenoleukodystrofie, ald, mutation, Addison's disease, peroxisome, fatty acids, VLCFA, diagnosis, ALDP, leukodystrophy, white matter, myelin, ZLKV |
| Description: | The adrenoleukodystrophy database serves as a catalog for ABCD1 mutations and provides information on X-ALD. |
| IP-address: | 195.20.11.38 |