This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Email citation

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 2008 Jul;9(3):225-6.

doi: 10.1007/s10048-008-0130-8. Epub 2008 May 8.

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

Lúcia Inês Macedo-Souza, Fernando Kok, Silvana Santos, Luciana Licinio, Karina Lezirovitz, Rafaella M P Nascimento, Clarissa Bueno, Marcília Martyn, Emília K E A Leão, Mayana Zatz

PMID: 18463901
DOI: 10.1007/s10048-008-0130-8

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

Lúcia Inês Macedo-Souza et al. Neurogenetics. 2008 Jul.

. 2008 Jul;9(3):225-6.

doi: 10.1007/s10048-008-0130-8. Epub 2008 May 8.

Authors

Lúcia Inês Macedo-Souza, Fernando Kok, Silvana Santos, Luciana Licinio, Karina Lezirovitz, Rafaella M P Nascimento, Clarissa Bueno, Marcília Martyn, Emília K E A Leão, Mayana Zatz

PMID: 18463901
DOI: 10.1007/s10048-008-0130-8

No abstract available

PubMed Disclaimer

Similar articles

Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A. Muglia M, et al. Neurogenetics. 2004 Feb;5(1):49-54. doi: 10.1007/s10048-003-0167-7. Epub 2003 Dec 5. Neurogenetics. 2004. PMID: 14658060
A new, X-linked endothelial corneal dystrophy.
Schmid E, Lisch W, Philipp W, Lechner S, Göttinger W, Schlötzer-Schrehardt U, Müller T, Utermann G, Janecke AR. Schmid E, et al. Am J Ophthalmol. 2006 Mar;141(3):478-487. doi: 10.1016/j.ajo.2005.10.020. Am J Ophthalmol. 2006. PMID: 16490493
A novel locus for X-linked congenital cataract on Xq24.
Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, Burdon KP. Craig JE, et al. Mol Vis. 2008 Apr 18;14:721-6. Mol Vis. 2008. PMID: 18431456 Free PMC article.
Molecular genetics of familial spastic paraplegia: a multitude of responsible genes.
Kobayashi H, Garcia CA, Alfonso G, Marks HG, Hoffman EP. Kobayashi H, et al. J Neurol Sci. 1996 May;137(2):131-8. doi: 10.1016/0022-510x(95)00349-7. J Neurol Sci. 1996. PMID: 8782167 Review.
The relationship of x-linked primary immune deficiencies and autoimmunity.
Pessach IM. Pessach IM. Curr Allergy Asthma Rep. 2010 Sep;10(5):311-9. doi: 10.1007/s11882-010-0127-x. Curr Allergy Asthma Rep. 2010. PMID: 20571932 Review.

See all similar articles

Cited by

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.
Fink JK. Fink JK. Acta Neuropathol. 2013 Sep;126(3):307-28. doi: 10.1007/s00401-013-1115-8. Epub 2013 Jul 30. Acta Neuropathol. 2013. PMID: 23897027 Free PMC article. Review.
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology.
Tesson C, Koht J, Stevanin G. Tesson C, et al. Hum Genet. 2015 Jun;134(6):511-38. doi: 10.1007/s00439-015-1536-7. Epub 2015 Mar 11. Hum Genet. 2015. PMID: 25758904 Free PMC article. Review.
Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.
de Souza PVS, de Rezende Pinto WBV, de Rezende Batistella GN, Bortholin T, Oliveira ASB. de Souza PVS, et al. Cerebellum. 2017 Apr;16(2):525-551. doi: 10.1007/s12311-016-0803-z. Cerebellum. 2017. PMID: 27271711 Review.
Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.
Braschinsky M, Tamm R, Beetz C, Sachez-Ferrero E, Raukas E, Lüüs SM, Gross-Paju K, Boillot C, Canzian F, Metspalu A, Haldre S. Braschinsky M, et al. BMC Neurol. 2010 Mar 9;10:17. doi: 10.1186/1471-2377-10-17. BMC Neurol. 2010. PMID: 20214791 Free PMC article.
SPG3A gene polymorphisms in hereditary spastic paraplegia.
Li T, Tu L, Zhang Q, Gu R, Wang Q, Wang B, Yao H, Qu X, Wang W, Tian J. Li T, et al. Int J Clin Exp Pathol. 2017 Sep 1;10(9):9760-9764. eCollection 2017. Int J Clin Exp Pathol. 2017. PMID: 31966859 Free PMC article.

See all "Cited by" articles

References

1. Prog Neurobiol. 2007 Feb;81(3):179-96 - PubMed
1. Nat Genet. 1994 Jul;7(3):351-2 - PubMed
1. Arch Neurol. 2003 Aug;60(8):1045-9 - PubMed
1. Am J Med Genet. 2000 Sep 4;94(1):5-8 - PubMed
1. Am J Med Genet. 2002 Aug 1;111(2):152-6 - PubMed

Publication types

Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Springer