AP-4 complex accessory subunit RUSC2 isoform 1 [Homo sapiens]

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Loss-of-function mutation in RUSC2 causes intellectual disability and secondary microcephaly. [Dev Med Child Neurol. 2016]
Loss-of-function mutation in RUSC2 causes intellectual disability and secondary microcephaly.
Alwadei AH, Benini R, Mahmoud A, Alasmari A, Kamsteeg EJ, Alfadhel M. Dev Med Child Neurol. 2016 Dec; 58(12):1317-1322. Epub 2016 Sep 9.
Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias. [Genes Chromosomes Cancer. 2014]
Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias.
Sarhadi VK, Lahti L, Scheinin I, Ellonen P, Kettunen E, Serra M, Scotlandi K, Picci P, Knuutila S. Genes Chromosomes Cancer. 2014 Jul; 53(7):579-88. Epub 2014 Mar 24.
Characterization of RUSC1 and RUSC2 genes in silico. [Oncol Rep. 2004]
Characterization of RUSC1 and RUSC2 genes in silico.
Katoh M, Katoh M. Oncol Rep. 2004 Oct; 12(4):933-8.

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AP-4 complex accessory subunit RUSC2 isoform 1 [Homo sapiens]
AP-4 complex accessory subunit RUSC2 isoform 1 [Homo sapiens]
gi|1519312076|ref|NP_055621.2|

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