| 1 | AP4B1, SPG47
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| Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47).
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| Bauer P, Leshinsky-Silver E, Blumkin L, Schlipf N, Schröder C, Schicks J, Lev D, Riess O, Lerman-Sagie T, Schöls L.
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| Neurogenetics. 2012
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| 2 | AP4B1, AP4DS, AP4E1, AP4S1, CPSQ5, CSPQ6
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| Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature.
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| Abou Jamra R, Philippe O, Raas-Rothschild A, Eck SH, Graf E, Buchert R, Borck G, Ekici A, Brockschmidt FF, Nöthen MM, Munnich A, Strom TM, Reis A, Colleaux L.
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| Am J Hum Genet 88(6):788-95. Epub 2011 May 27. 2011
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| 3 | AP4B1
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| Similar subunit interactions contribute to assembly of clathrin adaptor complexes and COPI complex: analysis using yeast three-hybrid system.
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| Takatsu H, Futatsumori M, Yoshino K, Yoshida Y, Shin HW, Nakayama K.
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| Biochem Biophys Res Commun. 284(4):1083-9. 2001
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| 4 | AP4B1, TFAP4, AP4M1
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| AP-4, a novel protein complex related to clathrin adaptors.
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| Dell'Angelica EC, et al.
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| J Biol Chem 274(11):7278-85. 1999
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| 5 | AP4B1, AP4E1, AP4M1, AP4S1
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| Characterization of a fourth adaptor-related protein complex.
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| Hirst J, Bright NA, Rous B, Robinson MS.
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| Mol Biol Cell 10(8):2787-802. 1999
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