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    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly

    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly 由 Myriam Srour, Fadi F. Hamdan, Ziv Gan‐Or, D. Labuda, Christina Nassif, Maryam Oskoui, Mali Gana‐Weisz, Avi Orr‐Urtreger, Guy A. Rouleau, Jacques L. Michaud

    出版 2015
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