A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency-Reference-Cited by-同舟云学术

A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency

Published:2014-12 Issue:1 Volume:15 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Jameel Muhammad,Klar Joakim,Tariq Muhammad,Moawia Abubakar,Altaf Malik Naveed,Seema Waseem Syeda,Abdullah Uzma,Naeem Khan Tahir,Raininko Raili,Baig Shahid Mahmood,Dahl Niklas

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/article/10.1186/s12881-014-0133-2/fulltext.html

Reference21 articles.

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2. Pakula AT, Van Naarden BK, Yeargin-Allsopp M: Cerebral palsy: classification and epidemiology. Phys Med Rehabil Clin N Am. 2009, 20 (3): 425-452. 10.1016/j.pmr.2009.06.001.

3. Costeff H: Estimated frequency of genetic and nongenetic causes of congenital idiopathic cerebral palsy in west Sweden. Ann Hum Genet. 2004, 68 (Pt 5): 515-520. 10.1046/j.1529-8817.2004.00105.x.

4. Graham EM, Ruis KA, Hartman AL, Northington FJ, Fox HE: A systematic review of the role of intrapartum hypoxia-ischemia in the causation of neonatal encephalopathy. Am J Obstet Gynecol. 2008, 199 (6): 587-595. 10.1016/j.ajog.2008.06.094.

5. Petterson B, Stanley F, Henderson D: Cerebral palsy in multiple births in Western Australia: genetic aspects. Am J Med Genet. 1990, 37 (3): 346-351. 10.1002/ajmg.1320370311.

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