A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.

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Title: A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.
Authors: Srour, M.1,2, Hamdan, F. F.2, Gan‐Or, Z.3,4, Labuda, D.2,5, Nassif, C.2, Oskoui, M.1, Gana‐Weisz, M.6, Orr‐Urtreger, A.6,7, Rouleau, G.A.3,4,8, Michaud, J.L.2,5,9
Source: Clinical Genetics. Jul2015, Vol. 88 Issue 1, pE1-E4. 4p.
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  Data: A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Jul2015, Vol. 88 Issue 1, pE1-E4. 4p.
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              Text: Jul2015
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