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

Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency

By Anichini Angelica   Fanin Marina   Vianey-Saban Christine   Cassandrini Denise   Fiorillo Chiara   Bruno Claudio   Angelini Corrado  

Neurological Research, Vol. 33, Iss. 1, 2011-01 ,pp. : 24-32

Maney Publishing

Access to resources Recommend Favorite

Human 2-macroglobulin: genotype-phenotype relation

By Birkenmeier G.   Muller R.   Huse K.   Forberg J.   Glaser C.   Hedrich H.   Nicklisch S.   Reichenbach A.  

Experimental Neurology, Vol. 184, Iss. 1, 2003-11 ,pp. : 153-161

Elsevier

Access to resources Recommend Favorite

Genotype–Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1 HMR spectroscopy and MRI measures

By Okuda D. T.  

Brain, Vol. 132, Iss. 1, 2009-01 ,pp. : 250-259

Oxford University Press

Access to resources Recommend Favorite

Genotype phenotype correlations in spinocerebellar ataxias (SCA)

By Dichgans J.   Klockgether T.  

Electroencephalography and Clinical Neurophysiology, Vol. 103, Iss. 1, 1997-07 ,pp. : 19-20

Elsevier

Access to resources Recommend Favorite