๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

โœ Scribed by Shao-Ming Wu; Constantine A. Stratakis; Connie H.Y. Chan; Karen M. Hallermeier; Carlos J. Bourdony; Owen M. Rennert; Wai-Yee Chan


Book ID
115639412
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
804 KB
Volume
64
Category
Article
ISSN
1096-7192

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Identification of a novel frameshift mut
โœ Abdelaziz Tlili; Ilhem Charfedine; Imed Lahmar; Zaineb Benzina; Ben Amor Mohamed ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 65 KB ๐Ÿ‘ 1 views

## Communicated by Henrik Dahl Approximately 80% of hereditary hearing loss is non-syndromic. Non-syndromic deafness is the most genetically heterogeneous trait. The most common and severe form of hereditary hearing impairment is autosomal recessive non-syndromic hearing loss (ARNSHL), accounting f