Homo sapiens neurite extension and migration factor (NEXMIF), mRNA

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[Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene]. [Zh Nevrol Psikhiatr Im S S Kor...]
[Epilepsy and other phenotypic features of X-linked intellectual disability caused by the mutations in the KIAA2022 gene].
Gamirova RG, Barkov AI, Shaimuchametova VA, Liukshina NG, Volkov IV, Tomenko TR, Rachmanina OA, Shestakova OI, Gorobets EA. Zh Nevrol Psikhiatr Im S S Korsakova. 2022; 122(9. Vyp. 2):14-20.
NEXMIF mutations in intellectual disability and epilepsy: A report of 2 cases and literature review. [Zhong Nan Da Xue Xue Bao Yi Xu...]
NEXMIF mutations in intellectual disability and epilepsy: A report of 2 cases and literature review.
Chen S, Deng X, Xiong J, Chen B, He F, Yang L, Yang L, Peng J, Yin F. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2022 Feb 28; 47(2):265-270.
NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent. [Am J Med Genet A. 2022]
NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent.
Langley E, Farach LS, Koenig MK, Northrup H, Rodriguez-Buritica DF, Mowrey K. Am J Med Genet A. 2022 Jun; 188(6):1688-1692. Epub 2022 Feb 10.

RefSeq protein product
See the reference protein sequence for neurite extension and migration factor (NP_001008537.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
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Taxonomy
Taxonomy sequences associated with Nucleotide record
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