Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | An autosomal recessive metabolic disorder due to a deficiency in expression of branching enzyme (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches. Clinical features are muscle hypotonia and cirrhosis. Death from liver disease usually occurs before age 2. (references) |
Source: compiled by the editor from various references; see credits. | |
Hexadecimal (or equivalents, 770AD-1900s) (references)47 4C 59 43 4F 47 45 4E 53 54 4F 52 41 47 45 44 49 53 45 41 53 45 54 59 50 45 49 56 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01000111 01001100 01011001 01000011 01001111 01000111 01000101 01001110 00100000 01010011 01010100 01001111 01010010 01000001 01000111 01000101 00100000 01000100 01001001 01010011 01000101 01000001 01010011 01000101 00100000 01010100 01011001 01010000 01000101 00100000 01001001 01010110 |
HTML Code (1990) (references)G L Y C O G E N   S T O R A G E   D I S E A S E   T Y P E   I V |
ISO 10646 (1991-1993) (references)0047 004C 0059 0043 004F 0047 0045 004E 0053 0054 004F 0052 0041 0047 0045 0044 0049 0053 0045 0041 0053 0045 0054 0059 0050 0045 0049 0056 |
Encryption (beginner's substitution cypher): (references)414659374941394825354495235413923843533935533925459503924356 |
| 1. Orthography 2. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
