Published Date: February 15, 2021

Full Text Article

A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype


Authors: Akella Radha Rama Devi, Shaik Mohammad Naushad, Romit Jain, Lokesh Lingappa


Clin Genet. 2021 May;99(5):744-745. doi: 10.1111/cge.13934. Epub 2021 Feb 14.

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PMID: 33586168DOI: 10.1111/cge.13934