WRN mutation

Mutation 000


Mutation description:

Molecular type: substitution deletion insertion

Nucleotide notation:

Protein notation:

Location: exon

Allelic status: compound heterozygous homozygous


Mutation synonyms

LSMD # = Monnat Unique Number: 000

Werner syndrome Registry #:

Huang et al. mutation #: n/a

Uhrhammer mutation #: n/a

OMIM mutant allele #: n/a

HGMD mutation #: n/a

Japanese mutation #: n/a


Supplementary information

Patient ethnicity data: n/a

Patient race data: n/a

Additional Notes: n/a


References

Published descriptions/references: [ ]