Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome-Reference-Cited by-同舟云学术

Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome

Published:2007-12 Issue:1-2 Volume:263 Page:100-106
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Rohkamm Barbara,Reilly Mary M.,Lochmüller Hanns,Schlotter-Weigel Beate,Barisic Nina,Schöls Ludger,Nicholson Garth,Pareyson Davide,Laurà Matilde,Janecke Andreas R.,Miltenberger-Miltenyi Gabriel,John Elisabeth,Fischer Carina,Grill Franz,Wakeling William,Davis Mary,Pieber Thomas R.,Auer-Grumbach Michaela

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference18 articles.

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2. Phenotypes of the N88S Berardinelli–Seip congenital lipodystrophy 2 mutation;Auer-Grumbach;Ann Neurol,2005

3. Autosomal dominant Charcot–Marie–Tooth axonal neuropathy mapped on chromosome 7p (CMT2D);Ionasescu;Hum Mol Genet,1996

4. Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot–Marie–Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15;Sambuughin;J Neurol Sci,1998

5. Familial spastic paraplegia with amyotrophy of the hands;Silver;Ann Hum Genet,1966

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