Literature DB >> 10066034

TGFA: exon-intron structure and evaluation as a candidate gene for Alström syndrome.

G B Collin, J D Marshall, J K Naggert, P M Nishina.   

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Year:  1999        PMID： 10066034     DOI： 10.1034/j.1399-0004.1999.550111.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  2 in total

1.  A novel variant site of Alstrom syndrome in a Chinese child: a case report.

Authors:  Rongrong Xu; Hua Zhou; Feng Fang; Liru Qiu; Xinglou Liu
Journal:  Transl Pediatr       Date:  2022-04

2.  Consensus clinical management guidelines for Alström syndrome.

Authors:  Natascia Tahani; Pietro Maffei; Hélène Dollfus; Richard Paisey; Diana Valverde; Gabriella Milan; Joan C Han; Francesca Favaretto; Shyam C Madathil; Charlotte Dawson; Matthew J Armstrong; Adrian T Warfield; Selma Düzenli; Clair A Francomano; Meral Gunay-Aygun; Francesca Dassie; Vincent Marion; Marina Valenti; Kerry Leeson-Beevers; Ann Chivers; Richard Steeds; Timothy Barrett; Tarekegn Geberhiwot
Journal:  Orphanet J Rare Dis       Date:  2020-09-21       Impact factor: 4.123
  2 in total

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