MITOCHONDRIAL DNA 8993 (NARP) MUTATION PRESENTING WITH A HETEROGENEOUS PHENOTYPE INCLUDING "CEREBRAL PALSY"
Guardat en:
FRYER, A., ET AL., MITOCHONDRIAL DNA 8993 (NARP) MUTATION PRESENTING WITH A HETEROGENEOUS PHENOTYPE INCLUDING "CEREBRAL PALSY". ARCHIVES OF DISEASE IN CHILDHOOD, Vol. 71, no. 5 (1994), p. 419-422.
Ref.
47809
Localització:
SIIS R.186
Palabras clave:
Discapacidad, Enfermedades congénitas, Parálisis cerebral
Discapacidad, Enfermedades congénitas, Parálisis cerebral
Ítems similars: MITOCHONDRIAL DNA 8993 (NARP) MUTATION PRESENTING WITH A HETEROGENEOUS PHENOTYPE INCLUDING "CEREBRAL PALSY"
- EMERGING RESEARCH IN MITOCHONDRIAL DISEASE
- PREVALENCE AND PATHOGENESIS OF CONGENITAL ANOMALIES IN CEREBRAL PALSY
- NEONATAL PRESENTATIONS OF MITOCHONDRIAL METABOLIC DISORDERS
- OTHER FACTORS/CONDITIONS ASSOCIATED WITH CEREBRAL PALSY
- THE OFFSPRING OF PEOPLE WITH CEREBRAL PALSY
- CONGENITAL ANOMALIES IN CHILDREN WITH CEREBRAL PALSY: A POPULATIONBASED RECORD LINKAGE STUDY