论文信息 - A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency - 字舞流文

A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency

Robert W. Taylor | M. O'sullivan | C. McMahon | I. Hargreaves | P. Goffrini | C. Alston | R. Mcfarland | S. Olpin | E. Blakely | M. Oláhová | Camilla Ceccatelli Berti | C. Nolli | Langping He | Robert W. Taylor