A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis. [electronic resource]
Producer: 20110506Description: 93-5 p. digitalISSN:- 1364-6753
- Aminopeptidases -- genetics
- Asian People -- genetics
- Base Sequence
- Child
- China
- DNA -- genetics
- Dipeptidyl-Peptidases and Tripeptidyl-Peptidases -- genetics
- Female
- Humans
- Male
- Mutation
- Neuronal Ceroid-Lipofuscinoses -- enzymology
- Pedigree
- RNA Splice Sites
- Serine Proteases -- genetics
- Tripeptidyl-Peptidase 1
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Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
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