SPG16 - Misplaced Pages

Genetic element in the species Homo sapiens

SPG16

Identifiers

SPG16, SPG, spastic paraplegia 16 (complicated, X-linked recessive)

External IDs

Species

Human

Mouse

Entrez


57760


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n a


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RefSeq (mRNA)


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RefSeq (protein)


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Location (UCSC)

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PubMed search

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Spastic paraplegia 16 (complicated, X-linked recessive) is a protein that in humans is encoded by the SPG16 gene.

References

Steinmüller R, Lantigua-Cruz A, Garcia-Garcia R, Kostrzewa M, Steinberger D, Müller U (August 1997). "Evidence of a third locus in X-linked recessive spastic paraplegia". Human Genetics. 100 (2): 287–9. doi:10.1007/s004390050507. PMID 9254866. S2CID 10378741.
Tamagaki A, Shima M, Tomita R, Okumura M, Shibata M, Morichika S, Kurahashi H, Giddings JC, Yoshioka A, Yokobayashi Y (September 2000). "Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2". American Journal of Medical Genetics. 94 (1): 5–8. doi:10.1002/1096-8628(20000904)94:1<5::AID-AJMG2>3.0.CO;2-O. PMID 10982474.
Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP (September 2000). "Novel syndromic form of X-linked complicated spastic paraplegia". American Journal of Medical Genetics. 94 (1): 1–4. doi:10.1002/1096-8628(20000904)94:1<1::AID-AJMG1>3.0.CO;2-V. PMID 10982473.

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