Deep sequencing reveals 50 novel genes for recessive cognitive disorders
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Published in Nature (London) (06.10.2011)
Published in Nature (London) (06.10.2011)
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Journal Article
CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling
Starokadomskyy, Petro, Gluck, Nathan, Li, Haiying, Chen, Baozhi, Wallis, Mathew, Maine, Gabriel N, Mao, Xicheng, Zaidi, Iram W, Hein, Marco Y, McDonald, Fiona J, Lenzner, Steffen, Zecha, Agnes, Ropers, Hans-Hilger, Kuss, Andreas W, McGaughran, Julie, Gecz, Jozef, Burstein, Ezra
Published in The Journal of clinical investigation (01.05.2013)
Published in The Journal of clinical investigation (01.05.2013)
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Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots
Kuss, Andreas Walter, Garshasbi, Masoud, Kahrizi, Kimia, Tzschach, Andreas, Behjati, Farkhondeh, Darvish, Hossein, Abbasi-Moheb, Lia, Puettmann, Lucia, Zecha, Agnes, Weißmann, Robert, Hu, Hao, Mohseni, Marzieh, Abedini, Seyedeh Sedigheh, Rajab, Anna, Hertzberg, Christoph, Wieczorek, Dagmar, Ullmann, Reinhard, Ghasemi-Firouzabadi, Saghar, Banihashemi, Susan, Arzhangi, Sanaz, Hadavi, Valeh, Bahrami-Monajemi, Gholamreza, Kasiri, Mahboubeh, Falah, Masoumeh, Nikuei, Pooneh, Dehghan, Atefeh, Sobhani, Masoumeh, Jamali, Payman, Ropers, Hans Hilger, Najmabadi, Hossein
Published in Human genetics (01.02.2011)
Published in Human genetics (01.02.2011)
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Journal Article
CCDC22 deficiency in humans blunts activation of proinflammatory NF-[kappa]B signaling
Starokadomskyy, Petro, Gluck, Nathan, Li, Haiying, Chen, Baozhi, Wallis, Mathew, Maine, Gabriel N, Mao, Xicheng, Zaidi, Iram W, Hein, Marco Y, McDonald, Fiona J, Lenzner, Steffen, Zecha, Agnes, Ropers, Hans-Hilger, Kuss, Andreas W, McGaughran, Julie, Gecz, Jozef, Burstein, Ezra
Published in The Journal of clinical investigation (01.05.2013)
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Published in The Journal of clinical investigation (01.05.2013)
Journal Article