Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7369
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Type: Journal article
Title: Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndrome
Author: Isbrandt, D.
Hopwood, J.
von Figura, K.
Peters, C.
Citation: Human Mutation, 1996; 7(4):361-363
Publisher: Wiley
Issue Date: 1996
ISSN: 1059-7794
1098-1004
Keywords: Humans
Mucopolysaccharidosis IV
Codon, Terminator
DNA Primers
Amino Acid Sequence
Base Sequence
Heterozygote
Frameshift Mutation
Open Reading Frames
Molecular Sequence Data
Child, Preschool
DOI: 10.1002/(SICI)1098-1004(1996)7:4<361::AID-HUMU12>3.0.CO;2-0
Appears in Collections:Aurora harvest 5
Paediatrics publications

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