Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease muscular dystrophy
Phenotype C0020255|hydrocephalus
Sentences 1
PubMedID- 26452345 The strongest indication that this mutation causes the phenotype in friesian horses is that the exact same nonsense mutation was found homozygously in a human muscular dystrophy patient with hydrocephalus by stevens et al.

Page: 1