Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly

Por Fabbro, Shay, Kahr, Walter H. A., Hinckley, Jesse, Wang, Kai, Moseley, Jack, Ryu, Gi-Yung, Nixon, Brie, White, James G., Bair, Thomas, Schutte, Brian, Di Paola, Jorge
Publicado em 2011

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

Por Kahr, Walter HA, Hinckley, Jesse, Li, Ling, Schwertz, Hansjörg, Christensen, Hilary, Rowley, Jesse W, Pluthero, Fred G, Urban, Denisa, Fabbro, Shay, Nixon, Brie, Gadzinski, Rick, Storck, Mike, Wang, Kai, Ryu, Gi-Yung, Jobe, Shawn M, Schutte, Brian C, Moseley, Jack, Loughran, Noeleen B, Parkinson, John, Weyrich, Andrew S, Paola, Jorge Di
Publicado no Nat Genet (2011)