Molecular genetic characterization of an X-linked form of Leigh's syndrome. [electronic resource]
Producer: 19930624Description: 652-5 p. digitalISSN:- 0364-5134
- Amino Acid Sequence
- Aspartic Acid
- Base Sequence
- Brain Stem -- pathology
- Cells, Cultured
- Cesarean Section
- Citrate (si)-Synthase -- metabolism
- DNA -- genetics
- Exons
- Fibroblasts -- pathology
- Gestational Age
- Humans
- Infant, Newborn
- Leigh Disease -- genetics
- Leukocytes -- physiology
- Male
- Mitochondria, Heart -- enzymology
- Mitochondria, Liver -- enzymology
- Molecular Sequence Data
- Necrosis
- Oligodeoxyribonucleotides
- Point Mutation
- Pyruvate Dehydrogenase Complex -- genetics
- Skin -- pathology
- X Chromosome
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.