Whole-exome sequencing identifies <i>ADRA2A</i> mutation in atypical familial partial lipodystrophy.

Garg, Abhimanyu; Sankella, Shireesha; Xing, Chao; Agarwal, Anil K

Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophy.

Garg, Abhimanyu; Sankella, Shireesha; Xing, Chao; Agarwal, Anil K.

Afiliação

Garg A; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, and Center for Human Nutrition.
Sankella S; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, and Center for Human Nutrition.
Xing C; Department of Clinical Sciences and McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, Texas, USA.
Agarwal AK; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, and Center for Human Nutrition.

JCI Insight ; 1(9)2016 Jun 16.

Article em En | MEDLINE | ID: mdl-27376152

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article