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Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency

✍ Scribed by Tommaso Fasano; Paolo Zanoni; Claudio Rabacchi; Livia Pisciotta; Elda Favari; Maria Pia Adorni; Patrick B. Deegan; Adrian Park; Thinn Hlaing; Michael D. Feher; Ben Jones; Asli Subasioglu Uzak; Fatih Kardas; Andrea Dardis; Annalisa Sechi; Bruno Bembi; Pietro Minuz; Stefano Bertolini; Franco Bernini; Sebastiano Calandra

Book ID: 118507166
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 399 KB
Volume: 107
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2012.08.005

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