Article
The genotype-phenotype correlation in Pompe disease.
American journal of medical genetics. Part C, Seminars in medical genetics - 15 Feb 2012
Kroos Marian, Hoogeveen-Westerveld Marianne, van der Ploeg Ans, Reuser Arnold J J
Abstract excerpt
Pompe disease is an autosomal recessive lysosomal glycogen storage disorder that is caused by acid α-glucosidase (GAA) deficiency and is due to pathogenic sequence variations in the corresponding GAA gene. The correlation between genotypes and phenotypes is strict, in that patients with the most severe phenotype, classic infantile Pompe disease, have two pathogenic mutations, one in each GAA allele, that prevent...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
