Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs.

Shaheen, R

Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs. [electronic resource] - Clinical genetics Jan 2011 - 60-70 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1399-0004

10.1111/j.1399-0004.2010.01498.x doi


Arabs
Child, Preschool
Cytogenetic Analysis
Female
Genetic Association Studies
Genetic Heterogeneity
Humans
Infant
Infant, Newborn
Male
Middle East
Mutation
Peroxisomal Disorders--ethnology
Peroxisomes--genetics
Sequence Analysis