Ali, R. H., & Umair, M. A novel Homozygous Mutation in SPTBN4 (Spectrin beta chain, non-erythrocytic 4) with syndromic neurodevelopmental phenotype in a consanguineous family of Saudi Origin. Discover STM Publishing Ltd.
Chicago Style (17th ed.) CitationAli, Raja Hussain, and Muhammad Umair. A Novel Homozygous Mutation in SPTBN4 (Spectrin Beta Chain, Non-erythrocytic 4) with Syndromic Neurodevelopmental Phenotype in a Consanguineous Family of Saudi Origin. Discover STM Publishing Ltd.
MLA (9th ed.) CitationAli, Raja Hussain, and Muhammad Umair. A Novel Homozygous Mutation in SPTBN4 (Spectrin Beta Chain, Non-erythrocytic 4) with Syndromic Neurodevelopmental Phenotype in a Consanguineous Family of Saudi Origin. Discover STM Publishing Ltd.
Warning: These citations may not always be 100% accurate.