ID

45187

Beschrijving

Principal Investigator: Yaniv Erlich, PhD, Whitehead Institute for Biomedical Research, Boston, MA, USA MeSH: Hereditary Spastic Paraplegias,Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000359 The study involves a single consanguineous Palestinian family with Hereditary Spastic Paraparesis (HSP). The affected individuals suffer from spasticity of the lower limbs and abnormal gait. Using exome sequencing and homozygosity mapping, our analysis implicated the causative mutation in the motor domain of KIF1A, a gene that functions in anterograde axonal transportation.

Link

dbGaP study = phs000359

Trefwoorden

Versies (2)
  1. 19-08-22 19-08-22 - Simon Heim
  2. 12-10-22 12-10-22 - Adrian Schulz
Houder van rechten

Yaniv Erlich, PhD, Whitehead Institute for Biomedical Research, Boston, MA, USA

Geüploaded op

12 oktober 2022

DOI

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Licentie

Creative Commons BY 4.0
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dbGaP phs000359 KIF1A Hereditary Spastic Paraparesis

Engels

Eligibility Criteria

4 Formulieren  
Inclusion and exclusion criteria
Beschrijving

Inclusion and exclusion criteria

The participants are part of a single family with HSP. The mother and the father are healthy and the two children are affected. We submit the exome sequencing of the father, mother, and one child, and the whole genome-genotyping of the two children.
Beschrijving

The participants are part of a single family with HSP. The mother and the father are healthy and the two children are affected. We submit the exome sequencing of the father, mother, and one child, and the whole genome-genotyping of the two children.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C0037773
UMLS CUI [1,3]
C0030551
UMLS CUI [1,4]
C3898900
UMLS CUI [1,5]
C0008059
UMLS CUI [1,6]
C0221423
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Similar models

Eligibility Criteria

4 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion and exclusion criteria
The participants are part of a single family with HSP. The mother and the father are healthy and the two children are affected. We submit the exome sequencing of the father, mother, and one child, and the whole genome-genotyping of the two children.
Item
The participants are part of a single family with HSP. The mother and the father are healthy and the two children are affected. We submit the exome sequencing of the father, mother, and one child, and the whole genome-genotyping of the two children.
boolean
C0015576 (UMLS CUI [1,1])
C0037773 (UMLS CUI [1,2])
C0030551 (UMLS CUI [1,3])
C3898900 (UMLS CUI [1,4])
C0008059 (UMLS CUI [1,5])
C0221423 (UMLS CUI [1,6])
Terug naar het begin van de pagina 

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