Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Shalini Thirukeswaran
Institutions:
Royal Children's Hospital,
The University of Melbourne,
Murdoch Children's Research Institute
Observed institutions:
Royal Children's Hospital,
The University of Melbourne,
Murdoch Children's Research Institute
OpenAlex ID:
A5005064833
The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy
2020
·
Lisa G. Riley
, Joëlle Rudinger‐Thirion
, et al.
·
Human Mutation
·
36
PDF
Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing
2019
·
Shalini Thirukeswaran
·
Minerva Access (University of Melbourne)
Show more works
View as search
Works count:
2
Citation count:
36
H-index:
1
I10-index:
1
Year
Topic
Type
