Search Results (12)

More Search Options

Match	Type	Why
Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia.	Academic Article	Why?
Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.	Academic Article	Why?
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.	Academic Article	Why?
Motor protein mutations cause a new form of hereditary spastic paraplegia.	Academic Article	Why?
Spastic Paraplegia, Hereditary	Concept	Why?
MitCHAP-60 and Hereditary Spastic Paraplegia SPG-13 Arise from an Inactive hsp60 Chaperonin that Fails to Fold the ATP Synthase ?-Subunit.	Academic Article	Why?
Huckaba, Thomas	Person	Why?
Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.	Academic Article	Why?
Bernal, Ricardo	Person	Why?
Gonzalez, Michael J	Person	Why?
Mottamal, Madhusoodanan	Person	Why?
Davidson, Michael	Person	Why?

Per Page

Page of 1

Search Criteria

Hereditary Spastic Paraplegia

Filter by Type

All (12)

People (5)

Research (6)

Concepts (1)

Click "Why?" to see why an item matched the search.

RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

For technical support please contact support