Talk:Ocular albinism type 1

Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Ocular albinism type 1.

PubMed provides review articles from the past five years (limit to free review articles)
The TRIP database provides clinical publications about evidence-based medicine.
Other potential sources include: Centre for Reviews and Dissemination and CDC

A fact from Ocular albinism type 1 appeared on Wikipedia's Main Page in the Did you know column on 29 October 2008, and was viewed approximately 1,735 times (disclaimer) (check views). The text of the entry was as follows:

Did you know... that Nettleship-Falls syndrome, the most common type of ocular albinism, may be caused by recessive mutations in the X chromosome?

A record of the entry may be seen at Wikipedia:Recent additions/2008/October.

Wikipedia

Medicine: Genetics / Ophthalmology Low‑importance

	Medicine portal This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources. Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine.MedicineWikipedia:WikiProject MedicineTemplate:WikiProject Medicinemedicine articles
Low	This article has been rated as Low-importance on the project's importance scale.
	This article is supported by the Medical genetics task force.
	This article is supported by the Ophthalmology task force.

note

Question: If this is X-linked (to me that means it is on the X chromosome), the how can it be EXCLUSIVELY MALE? Women are carriers, and a male with the disorder both have the "defective" X chromosome. Thus women may also have the disorder although most likely at a lower frequency. —Preceding unsigned comment added by 199.244.214.59 (talk) 14:35, 9 September 2009 (UTC)[reply]