Early endocrinological deficiencies can anticipate the diagnosis of mitochondrial diseases: Phenotype evolution of a rare MT-TG gene variant

被引：0

作者：

Mozzato, Chiara ^{[1
]}

Carecchio, Miryam ^{[2
]}

Salviati, Leonardo ^{[3
]}

Zeviani, Massimo ^{[4
]}

Guazzarotti, Laura ^{[5
]}

机构：

[1] Univ Padua, Dept Womens & Childrens Hlth, Padua, Italy

[2] Univ Padua, Dept Neurosci, Movement Disorders Unit, Padua, Italy

[3] Univ Hosp Padova, Dept Womens & Childrens Hlth, Clin Genet Unit, Padua, Italy

[4] Univ Padua, Dept Neurosci, Padua, Italy

[5] Univ Hosp Padova, Dept Womens & Childrens Hlth, Paediat Endocrinol Unit, Padua, Italy

来源：

HORMONE RESEARCH IN PAEDIATRICS | 2022年 / 95卷 / SUPPL 2期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

P1-335

引用

页码：328 / 329

页数：2