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-Reference-Cited by-同舟云学术

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

Published:1998-11 Issue:1 Volume:161 Page:23-28
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Sambuughin Nyamkhishig,Sivakumar Kumaraswamy,Selenge Badamjav,Suk Lee Hee,Friedlich Daniel,Baasanjav Damchaa,Dalakas Marinos C,Goldfarb Lev G

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference26 articles.

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2. Detection of Charcot-Marie-Tooth type 1A duplication by polymerase chain reaction;Blair;Clin. Chem.,1995

3. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders;Chance;Bailliére's Clinical Neurology,1994

4. Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p;Christodoulou;Hum. Mol. Genet.,1995

5. Faster sequential genetic linkage computations;Cottingham;Am. J. Hum. Genet.,1993

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