INTELLECTUAL DISABILITY AND ATAXIA: GENETIC COLLISIONS (REVIEW ARTICLE)

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KAZEMINASAB SOMAYEH; NAJMABADI HOSSEIN; KAHRIZI KIMIA

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Journal Paper

Paper Information

Journal: ARCHIVES OF IRANIAN MEDICINE Year:2018 | Volume:21 | Issue:1 Page(s): 29-40

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Title

INTELLECTUAL DISABILITY AND ATAXIA: GENETIC COLLISIONS (REVIEW ARTICLE)

Author(s)

KAZEMINASAB SOMAYEH | NAJMABADI HOSSEIN | KAHRIZI KIMIA | Issue Writer Certificate

Keywords

ATAXIA

CILIOGENESIS

ION CHANNELS

INTELLECTUAL DISABILITY

MITOCHONDRIA

Abstract

Intellectual disability (ID) is a common and highly heterogeneous neurodevelopmental disorder. The prevalence of ID is around 1%– 3% in the general population. ID is associated with a wide range of additional neurological disabilities and the results of various studies have disclosed the co-morbidity of ID and ATAXIA. The aim of this review is elucidation of the common molecular and cellular pathways in the etiology of ID and ATAXIA. Categorization of these genes with various cellular functions indicates several genetic collisions in the co-occurrence of ID and ATAXIA.

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APA: Copy

KAZEMINASAB, SOMAYEH, NAJMABADI, HOSSEIN, & KAHRIZI, KIMIA. (2018). INTELLECTUAL DISABILITY AND ATAXIA: GENETIC COLLISIONS (REVIEW ARTICLE). ARCHIVES OF IRANIAN MEDICINE, 21(1), 29-40. SID. https://sid.ir/paper/281593/en

Vancouver: Copy

KAZEMINASAB SOMAYEH, NAJMABADI HOSSEIN, KAHRIZI KIMIA. INTELLECTUAL DISABILITY AND ATAXIA: GENETIC COLLISIONS (REVIEW ARTICLE). ARCHIVES OF IRANIAN MEDICINE[Internet]. 2018;21(1):29-40. Available from: https://sid.ir/paper/281593/en

IEEE: Copy

SOMAYEH KAZEMINASAB, HOSSEIN NAJMABADI, and KIMIA KAHRIZI, “INTELLECTUAL DISABILITY AND ATAXIA: GENETIC COLLISIONS (REVIEW ARTICLE),” ARCHIVES OF IRANIAN MEDICINE, vol. 21, no. 1, pp. 29–40, 2018, [Online]. Available: https://sid.ir/paper/281593/en

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