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

fmrp
premature ovarian failure 1 gene
fragile x mental retardation 1 wt allele
fmr1 wt allele
mgc87458
pof
MainRecentTopDoctors

Recent Cases of Fraxa

Browse recently discussed Fraxa cases by specialists

Top Fraxa Doctors on Curofy

Top doctors who continously share their opinions on Fraxa
Valsad
619 followers

Surendranagar Chc Hospital Chuda Under Ccras Npcdcs Programme

Research Associate

Shree O H NAZAR Ayurvedic College Surat

BAMS

User Languages
Speaks English, Gujarati, Hindi
Kanpur
213 followers

Rani Sati Charitable

2 Years

BKHMC

BHMS

User Languages
Speaks English
Amritsar
29 followers
User Languages
Speaks English
Khed
64 followers
User Languages
Speaks English
Trivandrum
1313 followers

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)

User Languages
Speaks English, Hindi, Malyalam, Tamil, Arabic

Trending Cases