NEW GENE, NEW SKELETAL DYSPLASIA Intification and functional characterization of biallelic variants in PRKG2 as cause of a new Acromesomelic Dysplasia

Crespo, Francisca; Heath, Karen E.; Wadhwa, Saruchi; Heath, Mohammed Faruq; Kapoor, Seema; Nishimura, Gen; Amaka, C Offiah

doi:10.24217/2531-0151.21v1s4.00053

IBJ Plus

2021

DOI: 10.24217/2531-0151.21v1s4.00053

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NEW GENE, NEW SKELETAL DYSPLASIA Intification and functional characterization of biallelic variants in PRKG2 as cause of a new Acromesomelic Dysplasia

Francisca Crespo¹,

Karen E. Heath²,

Saruchi Wadhwa³

et al.

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NEW GENE, NEW SKELETAL DYSPLASIA Intification and functional characterization of biallelic variants in PRKG2 as cause of a new Acromesomelic Dysplasia

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