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Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant.
Garg, Abhimanyu; Keng, Wee-Teik; Chen, Zhenkang; Sathe, Adwait Amod; Xing, Chao; Kailasam, Pavithira Devi; Shao, Yanqiu; Lesner, Nicholas P; Llamas, Claire B; Agarwal, Anil K; Mishra, Prashant.
Afiliación
  • Garg A; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, Center for Human Nutrition, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Keng WT; Medical Genetics Department, Kuala Lumpur Hospital, Kuala Lumpur, Malaysia.
  • Chen Z; Children's Medical Center Research Institute.
  • Sathe AA; McDermott Center for Human Growth and Development, and.
  • Xing C; McDermott Center for Human Growth and Development, and.
  • Kailasam PD; Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Shao Y; Department of Pediatrics, Hospital Pakar Sultanah Fatimah, Johor, Malaysia.
  • Lesner NP; McDermott Center for Human Growth and Development, and.
  • Llamas CB; Children's Medical Center Research Institute.
  • Agarwal AK; Children's Medical Center Research Institute.
  • Mishra P; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, Center for Human Nutrition, UT Southwestern Medical Center, Dallas, Texas, USA.
J Clin Invest ; 132(23)2022 12 01.
Article en En | MEDLINE | ID: mdl-36282599
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Progeria / Lipodistrofia Límite: Adult / Humans Idioma: En Revista: J Clin Invest Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Progeria / Lipodistrofia Límite: Adult / Humans Idioma: En Revista: J Clin Invest Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos