Help FA in SA

This Blog was created for people interested in Friedreich Ataxia in South Australia. It provides a relaxing place to share and communicate what is going on, as well as links to FA groups and information from around the world. FAinSA is a non medical site for patients, families and friends of FA. All comments are a purely personal nature and do not replace advice from trained medical professionals

Friday, November 5, 2010

BabelFamily's interview with Ron Bartek (FARA) - part 4 of 7

http://www.youtube.com/watch?v=_V6mNAl4-qM
Posted by Laurel Hosking at 4:06 PM No comments:
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TRPing up the genome: tandem repeat polymorphisms as dynamic sources of genetic variability in health and disease. Hannan AJ.

http://www.ncbi.nlm.nih.gov/pubmed/21034672?dopt=Abstract
Posted by Laurel Hosking at 4:05 PM No comments:
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Friedreich's Ataxia Induced Pluripotent Stem Cells Model Intergenerational GAA⋅TTC Triplet Repeat Instability.

http://www.ncbi.nlm.nih.gov/pubmed/21040903?dopt=Abstract
Posted by Laurel Hosking at 4:04 PM No comments:
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Thursday, November 4, 2010

obitutuary

Aaron Kittel Aged 33
son of Sue and Joe, " left his body" on 3rd November 2010
Aaron has heroicly left his organs to research into Friedreich Ataxia

peace!

Posted by Laurel Hosking at 9:57 AM No comments:
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About FAinSA

Laurel Hosking
Gawler, South Australia, Australia
HI!. My son was diagnosed with FA in 2007. Since then I became aware how little is known about FA in South Australia. Early 2008 I chose to change this. This Blog was created to unite those with FA or touched by FA in South Australia
View my complete profile

Links

  • Help Friedreich Ataxia in South Australia
  • FA Babel Family ( Scientific Research and Fundraising)
  • FA Parents Group
  • FARA (USA)
  • FARA(A)
  • Friedreich Ataxia Network inc
  • International Network of Ataxia Friends

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