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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita |
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Titel: |
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita |
Auteur: |
Xue, Shifeng Maluenda, Jérôme Marguet, Florent Shboul, Mohammad Quevarec, Loïc Bonnard, Carine Ng, Alvin Yu Jin Tohari, Sumanty Tan, Thong Teck Kong, Mung Kei Monaghan, Kristin G. Cho, Megan T. Siskind, Carly E. Sampson, Jacinda B. Rocha, Carolina Tesi Alkazaleh, Fawaz Gonzales, Marie Rigonnot, Luc Whalen, Sandra Gut, Marta Gut, Ivo Bucourt, Martine Venkatesh, Byrappa Laquerrière, Annie Reversade, Bruno Melki, Judith |
Verschenen in: |
The American journal of human genetics |
Paginering: |
Jaargang 100 (2017) nr. 4 pagina's 7 p. |
Jaar: |
2017 |
Inhoud: |
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Uitgever: |
American Society of Human Genetics |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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