TY  - GEN
AU  - Jacobs,L J A M
AU  - Jongbloed,R J E
AU  - Wijburg,F A
AU  - de Klerk,J B C
AU  - Geraedts,J P M
AU  - Nijland,J G
AU  - Scholte,H R
AU  - de Coo,I F M
AU  - Smeets,H J M
TI  - Pearson syndrome and the role of deletion dimers and duplications in the mtDNA
SN  - 0141-8955
PY  - 2004///1012
KW  - Anemia
KW  - genetics
KW  - Bone Marrow Diseases
KW  - Child
KW  - Child, Preschool
KW  - DNA, Mitochondrial
KW  - Dimerization
KW  - Fatal Outcome
KW  - Female
KW  - Fibrosis
KW  - Gene Deletion
KW  - Gene Duplication
KW  - Gene Rearrangement
KW  - Genotype
KW  - Humans
KW  - Pancreatic Diseases
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1023/B:BOLI.0000016601.49372.18
ER  -