Gene table: search width pubmed_id = 10677302


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
Congenital muscular dystrophy - (AR)
2.45
10677302
? - (1q42)
* Congenital muscular dystrophy - MDC1B
* Congenital muscular dystrophy with merosin deficiency - MDC1B