Display Settings:

Format

Send to:

Choose Destination
Eur J Pediatr. 1982 Nov;139(3):210.

Phosphorylase kinase deficiency: severe glycogen storage disease with evidence of autosomal recessive mode of inheritance.

PMID:
6962066
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Write to the Help Desk