TY  - GEN
AU  - Al-Dirbashi,O Y
AU  - Shaheen,R
AU  - Al-Sayed,M
AU  - Al-Dosari,M
AU  - Makhseed,N
AU  - Abu Safieh,L
AU  - Santa,T
AU  - Meyer,B F
AU  - Shimozawa,N
AU  - Alkuraya,F S
TI  - Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations
SN  - 1552-4833
PY  - 2009///0730
KW  - Base Sequence
KW  - Fibroblasts
KW  - metabolism
KW  - Frameshift Mutation
KW  - Gene Rearrangement
KW  - Genetic Complementation Test
KW  - Humans
KW  - Infant
KW  - Membrane Proteins
KW  - deficiency
KW  - Molecular Sequence Data
KW  - Sequence Deletion
KW  - Zellweger Syndrome
KW  - genetics
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.a.32874
ER  -