Author response for "A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype"

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

doi:10.1111/cge.13934/v2/response1

2021

DOI: 10.1111/cge.13934/v2/response1

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Author response for "A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype"

Akella Radha Rama Devi¹,

Shaik Mohammad Naushad²,

Romit Jain³

et al.

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Author response for "A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype"

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