TY  - GEN
AU  - Schuelke,Markus
AU  - Detjen,Anne
AU  - van den Heuvel,Lambert
AU  - Korenke,Christoph
AU  - Janssen,Antoon
AU  - Smits,Arie
AU  - Trijbels,Frans
AU  - Smeitink,Jan
TI  - New nuclear encoded mitochondrial mutation illustrates pitfalls in prenatal diagnosis by biochemical methods
SN  - 0009-9147
PY  - 2002///0503
KW  - Acidosis, Lactic
KW  - congenital
KW  - Electron Transport Complex I
KW  - Female
KW  - Humans
KW  - Male
KW  - Mitochondria
KW  - genetics
KW  - NADH Dehydrogenase
KW  - NADH, NADPH Oxidoreductases
KW  - deficiency
KW  - Pedigree
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - methods
KW  - Proteins
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
ER  -