| 释义 |
- References
- Further reading
{{Orphan|date=January 2019}}{{Infobox_gene}}Spastic paraplegia 16 (complicated, X-linked recessive) is a protein that in humans is encoded by the SPG16 gene.[1] References 1. ^{{cite web | title = Entrez Gene: Spastic paraplegia 16 (complicated, X-linked recessive) | url = https://www.ncbi.nlm.nih.gov/gene/57760 }}
Further reading {{refbegin | 2}}- {{cite journal | vauthors = Steinmüller R, Lantigua-Cruz A, Garcia-Garcia R, Kostrzewa M, Steinberger D, Müller U | title = Evidence of a third locus in X-linked recessive spastic paraplegia | journal = Human Genetics | volume = 100 | issue = 2 | pages = 287–9 | date = August 1997 | pmid = 9254866 | doi = 10.1007/s004390050507 }}
- {{cite journal | vauthors = Tamagaki A, Shima M, Tomita R, Okumura M, Shibata M, Morichika S, Kurahashi H, Giddings JC, Yoshioka A, Yokobayashi Y | title = Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2 | journal = American Journal of Medical Genetics | volume = 94 | issue = 1 | pages = 5–8 | date = September 2000 | pmid = 10982474 | doi = 10.1002/1096-8628(20000904)94:1<5::AID-AJMG2>3.0.CO;2-O }}
- {{cite journal | vauthors = Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP | title = Novel syndromic form of X-linked complicated spastic paraplegia | journal = American Journal of Medical Genetics | volume = 94 | issue = 1 | pages = 1–4 | date = September 2000 | pmid = 10982473 | doi = 10.1002/1096-8628(20000904)94:1<1::AID-AJMG1>3.0.CO;2-V }}
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