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Browsing 2.Scientific Publications by Author "Srinivas Kovvali"

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Title: Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; peer review: 2 approved] Author: Desaraju Suresh Bhargav; Sreedevi, N.S; Swapna, N; Soumya Vivek; Srinivas Kovvali Year: 2017 Resource Type:Article

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