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

Authors :: Shaik Mohammad Naushad
Romit Jain
Lokesh Lingappa
Akella Radha Rama Devi
Publication Year :: 2021
Publisher :: Wiley, 2021.

Subjects :: Chondrodystrophy
medicine.medical_specialty
Endocrinology
Internal medicine
Rare case
medicine
Fatty acyl-CoA reductase
Biology
medicine.disease
Phenotype

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