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contentType Journal Article|Research Support, Non-U.S. Gov't
endingPage 784
issn 1098-3600
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publicationName Genetics in medicine : official journal of the American College of Medical Genetics
startingPage 778
bibliographicCitation Ansar M, Riazuddin S, Sarwar MT, Makrythanasis P, Paracha SA, Iqbal Z, Khan J, Assir MZ, Hussain M, Razzaq A, Polla DL, Taj AS, Holmgren A, Batool N, Misceo D, Iwaszkiewicz J, de Brouwer APM, Guipponi M, Hanquinet S, Zoete V, Santoni FA, Frengen E, Ahmed J, Riazuddin S, van Bokhoven H, Antonarakis SE. Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. Genet Med. 2018 Jul;20(7):778–84. doi: 10.1038/gim.2017.113. PMID: 28837161.
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title Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay
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