✦ LIBER ✦
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders
✍ Scribed by F Brancati; L Travaglini; D Zablocka; E Boltshauser; P Accorsi; G Montagna; JL Silhavy; G Barrano; E Bertini; F Emma; L Rigoli; The International JSRD Study Group; B Dallapiccola; JG Gleeson; EM Valente
- Book ID
- 110888648
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 149 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0009-9163
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