TY  - CHAP
M1  - Book, Section
TI  - Chapter 140. Disorders of Metabolism of Lysine, Hydroxylysine, and Related  Compounds
A1  - Goodman, Stephen I.
A2  - Rudolph, Colin D.
A2  - Rudolph, Abraham M.
A2  - Lister, George E.
A2  - First, Lewis R.
A2  - Gershon, Anne A.
PY  - 2011
T2  - Rudolph's Pediatrics, 22e
AB  - Deficiency  of  the  bifunctional  protein  alpha-aminoadipic  semialdehyde  synthase  causes  familial  hyperlysinemia.  The  clinical  significance  of  this  enzyme  deficiency  is  controversial.  Psychomotor  retardation  has  been  reported  in  many,  but  not  all,  affected  individuals.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/25
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=6725328
ER  -