Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland - Concepedia

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Publication | Open Access

Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland

DOI Full Paper Access

47

Citations

25

References

1999

Year

Laura Huopaniemi, Anne Rantala, Henrik Forsius, Mirja Somer, Albert de la Chapelle, Tiina Alitalo

European Journal of Human Genetics

OphthalmologyGenetic DisorderGeneticsX-linked Juvenile RetinoschisisHigh IncidenceWidespread Founder MutationsMedicine

References

	Year	Citations

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