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SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE
Known as:
SPG48
National Institutes of Health
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Related topics
Related topics
3 relations
Autosomal recessive inheritance
Lower limb muscle weakness
Urinary Incontinence
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2016
2016
Erratum: Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).
Neurology: Genetics
2016
Corpus ID: 261715808
[This corrects the article on p. e98 in vol. 2, PMID: 27606357.].