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H syndrome caused by a novel P324S mutation in SLC29A3 gene.
Bhandari, Molisha; Khullar, Geeti; Batra, Satyendra; Garg, Arpit; Khunger, Niti; Verma, Prashant; Singh, Amitabh; Misra, Ritu; Yadav, Amit Kumar.
Afiliação
  • Bhandari M; Department of Dermatology and Sexually Transmitted Diseases, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Khullar G; Department of Dermatology and Sexually Transmitted Diseases, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Batra S; Department of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Garg A; Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Khunger N; Department of Dermatology and Sexually Transmitted Diseases, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Verma P; Department of Dermatology and Sexually Transmitted Diseases, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Singh A; Department of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Misra R; Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
  • Yadav AK; Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Int J Dermatol ; 62(3): e138-e140, 2023 03.
Article em En | MEDLINE | ID: mdl-35556244
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperpigmentação / Contratura / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperpigmentação / Contratura / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2023 Tipo de documento: Article