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Diagnosis, treatment and genetic analysis of a case of Alstrom syndrome caused by compoud heterozygous mutation of ALMS1.
Yang, Hui-Jie; Li, De; Bai, Hui-Ling; Zhang, Ming; Huang, Jun; Yuan, Xiao-Qing.
Affiliation
  • Yang HJ; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
  • Li; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
  • Bai HL; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
  • Zhang M; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
  • Huang J; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
  • Yuan XQ; Department of Endocrinology, Changzhou Second People's Hospital affiliated to Nanjing Medical University, Changzhou 213000, China.
Yi Chuan ; 44(12): 1148-1157, 2022 Dec 20.
Article in En | MEDLINE | ID: mdl-36927560
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Full text: 1 Database: MEDLINE Main subject: Insulin Resistance / Deafness / Diabetes Mellitus / Fatty Liver / Alstrom Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Yi Chuan Journal subject: GENETICA Year: 2022 Type: Article Affiliation country: China
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Full text: 1 Database: MEDLINE Main subject: Insulin Resistance / Deafness / Diabetes Mellitus / Fatty Liver / Alstrom Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Yi Chuan Journal subject: GENETICA Year: 2022 Type: Article Affiliation country: China