TY  - GEN
AU  - Görgen-Pauly,U
AU  - Sperner,J
AU  - Reiss,I
AU  - Gehl,H B
AU  - Reusche,E
TI  - Familial pontocerebellar hypoplasia type I with anterior horn cell disease
SN  - 1090-3798
PY  - 2000///0421
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Atrophy
KW  - pathology
KW  - Cerebellum
KW  - abnormalities
KW  - Diagnosis, Differential
KW  - Fatal Outcome
KW  - Female
KW  - Humans
KW  - Infant, Newborn
KW  - Magnetic Resonance Imaging
KW  - Motor Neuron Disease
KW  - complications
KW  - Olivopontocerebellar Atrophies
KW  - Pedigree
KW  - Pons
KW  - Pregnancy
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1053/ejpn.1999.0177
ER  -