Hypomyelinating leukodystrophies - a molecular insight into the white matter pathology. [electronic resource]
Producer: 20170724Description: 293-304 p. digitalISSN:- 1399-0004
- Child
- Child, Preschool
- Diagnosis, Differential
- Genes, X-Linked
- Humans
- Leukoencephalopathies -- diagnosis
- Male
- X-Linked Intellectual Disability -- diagnosis
- Muscle Hypotonia -- diagnosis
- Muscular Atrophy -- diagnosis
- Mutation
- Myelin Sheath -- genetics
- Pedigree
- Pelizaeus-Merzbacher Disease -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article; Review; Research Support, Non-U.S. Gov't
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