TY  - GEN
AU  - Steinberg,S J
AU  - Snowden,A
AU  - Braverman,N E
AU  - Chen,L
AU  - Watkins,P A
AU  - Clayton,P T
AU  - Setchell,K D R
AU  - Heubi,J E
AU  - Raymond,G V
AU  - Moser,A B
AU  - Moser,H W
TI  - A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts
SN  - 1573-2665
PY  - 2009///0522
KW  - Adolescent
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Cells, Cultured
KW  - Female
KW  - Fibroblasts
KW  - metabolism
KW  - Humans
KW  - Molecular Sequence Data
KW  - Mutation
KW  - physiology
KW  - Pedigree
KW  - Peroxins
KW  - Peroxisomes
KW  - chemistry
KW  - Receptors, Cytoplasmic and Nuclear
KW  - genetics
KW  - Zellweger Syndrome
KW  - diagnosis
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1007/s10545-008-0969-8
ER  -