Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.

Boylan, K B

Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance. [electronic resource] - Annals of neurology Sep 1992 - 404-7 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0364-5134

10.1002/ana.410320318 doi


Adult
Female
Genes, Dominant
Humans
Infant
Male
Muscular Atrophy, Spinal--complications
Pedigree
Spinal Muscular Atrophies of Childhood--complications