Lowe syndrome

Orphanet Journal of Rare Diseases

Volumn 1, Issue 1, 2006, Pages

  Loi, Mario ^a  

^a BROTZU HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

OCRL PROTEIN, HUMAN; PHOSPHATASE; PHOSPHATIDYLINOSITOL;

ADOLESCENT; ADULT; CENTRAL NERVOUS SYSTEM DISEASE; CHILD; DIFFERENTIAL DIAGNOSIS; EYE DISEASE; FEMALE; GENETICS; HETEROZYGOTE DETECTION; HUMAN; INFANT; KIDNEY DISEASE; LOWE SYNDROME; METHODOLOGY; MIDDLE AGED; NEWBORN; PREGNANCY; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; PROGNOSIS; QUALITY OF LIFE; REVIEW;

ADOLESCENT; ADULT; CENTRAL NERVOUS SYSTEM DISEASES; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; EYE DISEASES; FEMALE; HETEROZYGOTE DETECTION; HUMANS; INFANT; INFANT, NEWBORN; KIDNEY DISEASES; MIDDLE AGED; OCULOCEREBRORENAL SYNDROME; PHOSPHATIDYLINOSITOLS; PHOSPHORIC MONOESTER HYDROLASES; PREGNANCY; PRENATAL DIAGNOSIS; PROGNOSIS; QUALITY OF LIFE; YOUNG ADULT;

EID: 33845600615     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-1-16     Document Type: Review

References (25)

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