all of them
Zellweger syndrome is autosomal recessive.
#21
chromosome 4
The chromosomes which are affected in Turner's Syndrome is the sex chromosomes. A normal female individual has 2 X sex chromosomes. In Turner's Syndrome, a woman only has one X chromosome and is missing the other. Thus, a woman with Turner's Syndrome has the sex chromosomes X0.
chromosome 21
There is no cure for Zellweger syndrome and treatment is based solely on lessening the symptoms and supporting the involved organs.
The incidence of Zellweger syndrome worldwide is roughly one in 100,000 births.
Zellweger syndrome is caused by mutations in any one of several different genes involved in the function of the peroxisome
peroxisomes
Typically, babies with Zellweger syndrome have severe weakness, hyptonia (loss of muscle tone), and often have neonatal seizures
Zellweger syndrome is caused by mutations in any one of at least 12 genes ; mutations in the PEX1 gene are the most common cause. It is inherited in an autosomal recessive manner. There is no cure for Zellweger syndrome; treatment is generally symptomatic and supportive.
Either chromosome 13 or 7. Mostly 13