TY  - GEN
AU  - Korinthenberg,R
AU  - Sauer,M
AU  - Ketelsen,U P
AU  - Hanemann,C O
AU  - Stoll,G
AU  - Graf,M
AU  - Baborie,A
AU  - Volk,B
AU  - Wirth,B
AU  - Rudnik-Schöneborn,S
AU  - Zerres,K
TI  - Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region
SN  - 0364-5134
PY  - 1997///1016
KW  - Axons
KW  - pathology
KW  - Brain Stem
KW  - Chromosomes, Human, Pair 5
KW  - Female
KW  - Gene Deletion
KW  - Hereditary Sensory and Autonomic Neuropathies
KW  - complications
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Microscopy, Electron
KW  - Muscle, Skeletal
KW  - ultrastructure
KW  - Neurons, Afferent
KW  - Phenotype
KW  - Spinal Muscular Atrophies of Childhood
KW  - Sural Nerve
N1  - Publication Type: Case Reports; Comparative Study; Journal Article
UR  - https://doi.org/10.1002/ana.410420314
ER  -