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A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype.
A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype.
2021
Akella Radha Rama Devi
Shaik Mohammad Naushad
Romit Jain
Lokesh Lingappa
Keywords:
Fatty acyl-CoA reductase
rare case
Phenotype
Chondrodystrophy
Biochemistry
Biology
Correction
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