Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.
Monogenic human disorders have been used as paradigms for complex genetic disease and as tools for establishing important insights into mechanisms of gene regulation and transcriptional control. Maturity-onset diabetes of the young (MODY) is a monogenic dominantly inherited form of diabetes that is...
Hlavní autoři: | Gloyn, A, Ellard, S, Shepherd, M, Howell, RT, Parry, E, Jefferson, A, Levy, E, Hattersley, A |
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Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2002
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