Gene table: search width pubmed_id = 22522420


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Muscular dystrophy-dystroglycanopathy (Congenital with brain and eyes anomlies), type A7 - (AR)
2.24
22522420
22522421
CRPPA (7p21.2-p21.1)
Isoprenoid synthase domain containing protein
* LGMDR20 - LGMDR20
* Walker-Warburg syndrome (WWS) - MDDGA7