Biallelic start loss variant, c. <scp>1A</scp>  &gt; G in <scp> <i>GCSH</i> </scp> is associated with variant nonketotic hyperglycinemia

Purvi Majethia(Manipal Academy of Higher Education), Anju Shukla(Manipal Academy of Higher Education), Katta M. Girisha(Manipal Academy of Higher Education), Puneeth H. Somashekar(Manipal Academy of Higher Education), Rajagopal Kadavigere(Manipal Academy of Higher Education), Malavika Hebbar(Manipal Academy of Higher Education), B. K. Praveen(Father Muller Medical College Hospital)
Clinical Genetics
April 23, 2021
Cited by 9


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