Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
<p>Abstract</p> <p>Background</p> <p>Imerslund-Gräsbeck syndrome (IGS) was described just over 50 years ago by Olga Imerslund and Ralph Gräsbeck and colleagues. IGS is caused by specific malabsorption of cobalamin (Cbl) due to bi-allelic mutations in either the cubilin...
Váldodahkkit: | , , , , , , |
---|---|
Materiálatiipa: | Artihkal |
Giella: | English |
Almmustuhtton: |
BMC
2011-11-01
|
Ráidu: | Orphanet Journal of Rare Diseases |
Fáttát: | |
Liŋkkat: | http://www.ojrd.com/content/6/1/74 |