TY  - GEN
AU  - Shaheen,R
AU  - Al-Dirbashi,O Y
AU  - Al-Hassnan,Z N
AU  - Al-Owain,M
AU  - Makhsheed,N
AU  - Basheeri,F
AU  - Seidahmed,M Z
AU  - Salih,M A M
AU  - Faqih,E
AU  - Zaidan,H
AU  - Al-Sayed,M
AU  - Rahbeeni,Z
AU  - Al-Sheddi,T
AU  - Hashem,M
AU  - Kurdi,W
AU  - Shimozawa,N
AU  - Alkuraya,F S
TI  - Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
SN  - 1399-0004
PY  - 2011///0321
KW  - Arabs
KW  - Child, Preschool
KW  - Cytogenetic Analysis
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Heterogeneity
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Middle East
KW  - Mutation
KW  - Peroxisomal Disorders
KW  - ethnology
KW  - Peroxisomes
KW  - genetics
KW  - Sequence Analysis
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2010.01498.x
ER  -