Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

Autor: Ansar, Muhammad, Riazuddin, Saima, Sarwar, Muhammad Tahir, Makrythanasis, Periklis, Paracha, Sohail Aziz, Iqbal, Zafar, Khan, Jamshed, Assir, Muhammad Zaman, Hussain, Mureed, Razzaq, Attia, Polla, Daniel Lôpo, Taj, Abid Sohail, Holmgren, Asbjørn, Batool, Naila, Misceo, Doriana, Iwaszkiewicz, Justyna, de Brouwer, Arjan P.M., Guipponi, Michel, Hanquinet, Sylviane, Zoete, Vincent, Santoni, Federico A., Frengen, Eirik, Ahmed, Jawad, Riazuddin, Sheikh, Van Bokhoven, Hans, Antonarakis, Stylianos E.

Publikováno v: Ansar, Muhammad Riazuddin, Saima Sarwar, Muhammad Tahir Makrythanasis, Periklis Paracha, Sohail Aziz Iqbal, Zafar Khan, Jamshed Assir, Muhammad Zaman Hussain, Mureed Razzaq, Attia Polla, Daniel Lôpo Taj, Abid Sohail Holmgren, Asbjørn Batool, Naila Misceo, Doriana Iwaszkiewicz, Justyna de Brouwer, Arjan P.M. Guipponi, Michel Hanquinet, Sylviane Zoete, Vincent Santoni, Federico A. Frengen, Eirik Ahmed, Jawad Riazuddin, Sheikh Van Bokhoven, Hans Antonarakis, Stylianos E. . Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. Genetics in Medicine. 2017
Genetics in Medicine

Externí odkaz: http://hdl.handle.net/10852/63293
https://www.duo.uio.no/bitstream/handle/10852/63293/1/LINGO1.pdf

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Biallelic variants in LINGO1are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

Autor: Ansar, Muhammad, Riazuddin, Saima, Sarwar, Muhammad Tahir, Makrythanasis, Periklis, Paracha, Sohail Aziz, Iqbal, Zafar, Khan, Jamshed, Assir, Muhammad Zaman, Hussain, Mureed, Razzaq, Attia, Polla, Daniel Lôpo, Taj, Abid Sohail, Holmgren, Asbjørn, Batool, Naila, Misceo, Doriana, Iwaszkiewicz, Justyna, de Brouwer, Arjan P.M., Guipponi, Michel, Hanquinet, Sylviane, Zoete, Vincent, Santoni, Federico A., Frengen, Eirik, Ahmed, Jawad, Riazuddin, Sheikh, van Bokhoven, Hans, Antonarakis, Stylianos E.

Publikováno v: Genetics in Medicine; July 2018, Vol. 20 Issue: 7 p778-784, 7p

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