Related content

Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination

By Wolf Nicole   Cundall Maria   Rutland Paul   Rosser Elisabeth   Surtees Robert   Benton Sarah   Chong Wui   Malcolm Sue   Ebinger Friedrich   Bitner-Glindzicz Maria   Woodward Karen  

Neurogenetics, Vol. 8, Iss. 1, 2007-01 ,pp. : 39-44

Springer Publishing Company

Access to resources Recommend Favorite

Magnetic stimulation of the corticospinal tracts in Pelizaeus-Merzbacher disease

By Nezu A.   Kimura S.   Takeshita S.   Osaka H.   Tanaka M.  

Electroencephalography and Clinical Neurophysiology/ Evoked Potentials Section, Vol. 108, Iss. 5, 1998-09 ,pp. : 446-448

Elsevier

Access to resources Recommend Favorite

Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus–Merzbacher disease

By Wolf Nicole I.  

Brain, Vol. 128, Iss. 4, 2005-04 ,pp. : 743-751

Oxford University Press

Access to resources Recommend Favorite

A large deletion and novel point mutations in the calpain 3 gene ( CAPN3 ) in Bulgarian LGMD2A patients

By Todorova Albena   Georgieva Bilyana   Tournev Ivailo   Todorov Tihomir   Bogdanova Nadja   Mitev Vanyo   Mueller Clemens   Kremensky Ivo   Horst Jürgen  

Neurogenetics, Vol. 8, Iss. 3, 2007-08 ,pp. : 225-229

Springer Publishing Company

Access to resources Recommend Favorite

A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease

By Züchner S.  

Brain, Vol. 126, Iss. 4, 2003-04 ,pp. : 920-927

Oxford University Press

Access to resources Recommend Favorite