TY  - GEN
AU  - Boylan,K B
AU  - Cornblath,D R
TI  - Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance
SN  - 0364-5134
PY  - 1992///1113
KW  - Adult
KW  - Female
KW  - Genes, Dominant
KW  - Humans
KW  - Infant
KW  - Male
KW  - Muscular Atrophy, Spinal
KW  - complications
KW  - Pedigree
KW  - Spinal Muscular Atrophies of Childhood
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ana.410320318
ER  -