Friedreich’s Ataxia-A Case Report
Friedrich’s ataxia (FA) is an autosomal recessive disorder. It is the most common cause of inherited ataxia. It affects approximately 1-2 persons per 100,000 population.[i] It occurs due to a mutation that results in the homozygous expansion of Guanosine Adenine Adenine trinucleotide (GAAT) repeat u...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Rawalpindi Medical University
2018-11-01
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| Series: | Journal of Rawalpindi Medical College |
| Online Access: | https://www.journalrmc.com/index.php/JRMC/article/view/977 |