Fraxa
Human FMR1 wild-type allele is located in the vicinity of Xq27.3 and is approximately 39 kb in length. This allele, which encodes fragile X mental retardation protein 1, may play a role in the mediation of mRNA transport. Amplification of a trinucleotide repeat (CGG) within the gene is associated with fragile X syndrome.
Disease Alternative Name
Recent Cases of Fraxa
Browse recently discussed Fraxa cases by specialistsTop Fraxa Doctors on Curofy
Top doctors who continously share their opinions on Fraxa
Surendranagar Chc Hospital Chuda Under Ccras Npcdcs Programme
Research Associate
Shree O H NAZAR Ayurvedic College Surat
BAMS
Rani Sati Charitable
2 Years
BKHMC
BHMS
Kerala Institute of Medical Sciences
Professor and Senior Consultant Neurology
Medical College Thiruvananthapuram
MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
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