File:Inheritance pattern in Huntington's Disease.jpeg: Difference between revisions
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Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome. | Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome. | ||
'''mHTT:''' Mutant huntingtin'' | |||
'''Red squares:''' HD affected offspring | |||
Revision as of 01:23, 13 October 2011
Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome.
mHTT: Mutant huntingtin
Red squares: HD affected offspring
Illustration by: z3290270
Inspiration: Yale Madical group - Yale School of Medicine
http://www.yalemedicalgroup.org/stw/Page.asp?PageID=STW025754
Beginning six months after publication, I z3290270 grant the public the non-exclusive right to copy, distribute, or display the Work under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/ and http://creativecommons.org/licenses/by-nc-sa/3.0/legalcode
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current | 12:24, 22 September 2011 | ![]() | 531 × 284 (15 KB) | Z3290270 (talk | contribs) | Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome. Illustration by: z3290270 Inspiration: Yale Madical group - Yale Sc |
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