Old Web
English
Sign In
Acemap
>
Paper
>
A Novel GHR Mutation, c.439+1g[gt]a; in a Family with Laron Syndrome
A Novel GHR Mutation, c.439+1g[gt]a; in a Family with Laron Syndrome
2014
Mona Attia
Atef Abeer
Ibrahim Makarem
Malcolm Donaldson
Lou Metherell
Sameh Tawfik
Wafaa Dowedar
Keywords:
Laron syndrome
Cancer research
Mutation
Growth hormone receptor
Biology
Internal medicine
Endocrinology
Correction
Source
Cite
Save
Machine Reading By IdeaReader
0
References
0
Citations
NaN
KQI
[]