Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing.

Authors:
Kumar KR; Wali GM; Kamate M; Wali G; Minoche AE and 7 more

Journal:
Neurogenetics

Publication Year: 2016

DOI:
10.1007/s10048-016-0495-z

PMCID:
PMC5061846

PMID:
27679996

View on PubMed View on PMC View Publisher
Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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Evidence found in paper:

"Conflict of interest The authors declare that they have no conflict of interest. Disclosures K.R.K. received honoraria from UCB Australia Pty Ltd. and Novartis Pharmaceuticals."

Evidence found in paper:

"Funding This study was funded by the Bushell Travelling Fellowship in Medicine or the Allied Sciences (The Royal Australasian College of Physicians Foundation). K.R.K. is supported by an NHMRC Early Career Fellowship, the Douglas Piper Fellowship from the Royal North Shore Hospital Scholarship Program, a Ramsay Research and Teaching Fund Knowledge Discovery Project (Biomedical Research). C.M.S. has been awarded a Brain Foundation grant and an NHMRC Practitioner Fellowship (#1008433). M.J.C. holds an Early Career Fellowship from Cancer Institute NSW (13/ECF/1-46 )."

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Last Updated: Aug 05, 2025